Three-dimensional boron-rich clusters
Novel three-dimensional molecular clusters and methods of their synthesis are provided. The three-dimensional molecular clusters may be perfunctionalized polyhedral boranes and carboranes. The three-dimensional clusters may be configured to manipulate the photophysical properties of other materials, including, for example, for use as photooxidants or as components in organic light-emitting diode materials. Methods are also provided for synthesizing and perfunctionalizing such three-dimensional clusters. The three-dimensional clusters may also be configured for use as organomimetic materials.
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The present invention generally relates to three-dimensional boron-rich clusters, the use of such clusters as substrates in a variety of photophysical processes and biomimetic functions, and methods of their manufacture, and of the manufacture of atomically precise nanoparticles therefrom.
BACKGROUNDPolyhedral carboranes are boron-rich molecular clusters that are often described as three-dimensional (3D) analogs to benzene. (See, e.g., Grimes, R. N. Carboranes, 2nd ed.; Elsevier: Oxford, 2011; and Spokoyny, A. M. Pure Appl. Chem. 2013, 85, 903, the disclosures of which are incorporated herein by reference.) Their unique delocalized 3D aromatic bonding, high stability, and potential for site-selective functionalization make them attractive building blocks for tunable pharmacophores, unique ligand scaffolds, and building blocks for materials applications. (See, e.g., Issa, F. et al., Chem. Rev. 2011, 111, 5701; McArthur, S. G. et al., Inorg. Chem. Front. 2015, 2, 1101; Bohling, L. et al., Eur. J. Inorg. Chem. 2016, 2016, 403; Jude, H., J. Am. Chem. Soc. 2005, 127, 12131; Farha, O. K. et al., J. Am. Chem. Soc. 2007, 129, 12680; Thomas, J. C. et al., Chem. Mater. 2015, 27, 5425; Yao, Z.-J. et al., J. Organomet. Chem. 2015, 798, 274; Douvris, C. & Ozerov, O. V., Science 2008, 321, 1188; Julius, R. L. et al., Proc. Natl. Acad. Sci. U.S.A 2007, 104, 4808; Endo, Y. et al., Itai, A. Chem. Biol. 2001, 8, 341; Lugo, C. A. et al., Inorg. Chem. 2015, 54, 2094; Shi, C. et al., Angew. Chem. 2013, 125, 13676; Lee, Y.-H. et al., J. Am. Chem. Soc. 2015, 137, 8018; and Joost, M. et al., J. Am. Chem. Soc. 2014, 136, 14654, the disclosures of which are incorporated herein by reference.)
SUMMARY OF THE INVENTIONNovel three-dimensional molecular clusters and methods of their synthesis are provided.
Various embodiments are directed to metal-free photooxidants comprising an icosahedral dodecaborate consisting of B12(OR)12 where R is an alkyl, unsubstituted, or substituted benzyl substituent.
In some such embodiments R is at least one of either an alkyl, substituted or unsubstituted benzyl substituent.
Other embodiments are directed to methods for photo-mediated (co)polymerization including:
-
- introducing a solution of a monomer and an icosahedral dodecaborate consisting of B12(OR)12 where R is an alkyl, unsubstituted, or substituted benzyl substituent; and
- illuminating the solution with an energetic emission.
In some such embodiments R is at least one of either an alkyl, substituted or unsubstituted benzyl substituent.
In other such embodiments the monomer(s) contains an alkene or epoxide.
In still other such embodiments the monomer(s) is selected from the group of substituted or unsubstituted styrenes, terpenes, cycloaliphatic epoxides, norbornenes, vinyl ethers, vinyl esters, methacrylates, acrylamides, hydrocarbons, maleic anhydrides, and various derivatives of molecules containing either activated or unactivated alkenes, or epoxides.
Still other embodiments are directed to a transition metal complex ligands including a 1, 1′-bis(o-carborane) consisting of [(C2H10B10)−]2.
Yet other embodiments are directed a transition metal complex ligands including a substituted 1, 1′-bis(o-carborane) consisting of (C2H9B10R2)2, where R is selected from the group consisting of: alkane, alkene, alkyne, alcohol, aryl, ether, halide, aldehyde, carboxylic acid, ester, amide, amine, nitrile, isocyanate, thiol and arene.
In some such embodiments the ligand is coordinated with a transition metal (M) at the CH group, and wherein the transition metal is selected from the group consisting of: Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ru, Rh, Pd, Ag, Re, Os, Ir, Pt and Au.
In other such embodiments the transition metal complex ligand further includes a bidentate ligand containing two N-M bonds.
In still other such embodiments the transition metal complex ligand further includes a monoanionic ligand containing a C-M or B-M bond.
In yet other such embodiments the monoanionic ligand is an acetylacetone.
In still yet other such embodiments the transition metal complex ligands may be used a dopants in organic light emitting diode materials.
Still yet other embodiments are directed to transition metal complex carboranyl-aryl ligands consisting of C2H8B10R2X,
where R is selected from the group consisting of: alkane, alkene, alkyne, alcohol, aryl, ether, halide, aldehyde, carboxylic acid, ester, amide, amine, nitrile, isocyanate, thiol and arene; and
where X is a substituted or unsubstituted aryl.
In some such embodiments the aryl is a pyridine.
Still yet other embodiments are directed to molecular scaffolds for forming atomically precise nanomolecules comprising an icosahedral dodecaborate consisting of B12(OR)12,
where R is a perfluoroaryl terminated linker.
In some such embodiments the dodecaborate is perfunctionalized with one or more alkyl or substituted aromatic perfunctionalization groups, and each of the perfluoraryl terminated linkers is attached to the dodecaborate through said perfunctionalization groups.
In other such embodiments one or more of the fluorine atoms of the perfluoroaryl terminated linkers is substituted with a thiol-containing molecule or macromolecule.
In still other such embodiments the thiol-containing macromolecule is a peptide such that the molecular scaffold is an organomimetic cluster nanomolecule.
In yet other such embodiments the molecular scaffold is PEGylated.
In still yet other such embodiments the thiol-containing molecules are recognition moieties.
In still yet other such embodiments the recognition moieties are glycoconjugates.
In still yet other such embodiments the glycoconjugates are linked with one or more molecules selected from the group consisting of proteins, peptides, lipid and saccharides.
In still yet other such embodiments the molecular scaffold forms an organomimetic cluster nanomolecule that functions as one of an antibody, protein, histone or viral mimic.
In still yet other such embodiments the molecular scaffold further comprises a viral scaffold and at least one fluorescent moiety, and wherein the molecular scaffold operates as a viral assay.
In still yet other such embodiments the viral scaffold is a gp41 viral scaffold.
In still yet other such embodiments the histone mimic comprises a periodic arrangement of cationic lysine residues separated by one or more helix-promoting hydrophobic amino acids.
Still yet other embodiments are directed to methods for forming atomically precise nanomolecules including:
providing an icosahedral dodecaborate scaffold consisting of B12(OR)12 appending one or more of the hydrogens on the dodecaborate scaffold with one or more perfluoroaryl terminated linkers;
conjugating one or more thiol containing molecules or macromolecules onto one or more of the perfluoraryl terminated linkers a nucleophilic aromatic substitution.
In some such embodiments the method further includes perfunctionalizing the dodecaborate scaffold with one or more alkyl or substituted aromatic perfunctionalization groups prior to appending the one or more perfluoraryl terminate linkers thereto.
Still yet other embodiments are directed to a covalent organic framework comprising two-dimensional carborane-containing polymer sheets.
In some such embodiments a plurality of receptor molecules are appended to the covalent organic framework.
In other such embodiments the receptor molecules are sugars or peptides.
Still yet other embodiments are directed to a method of forming a covalent organic framework including:
-
- providing a plurality of carboranes;
- forming a plurality of difunctionalized cyanocarbones therefrom via acid-mediated trimerization;
- forming a two-dimensional carborane-containing polymer sheet via an ionothermal polymerization; and
- functionalizing one or more of the carbon-hydrogen vertices of the two dimensional carborane-containing polymer sheet.
In some such embodiments the functionalization comprises appending one or more receptor molecules onto the carbon-hydrogen vertices.
Additional embodiments and features are set forth in part in the description that follows, and in part will become apparent to those skilled in the art upon examination of the specification or may be learned by the practice of the invention. A further understanding of the nature and advantages of the present invention may be realized by reference to the remaining portions of the specification and the drawings, which forms a part of this disclosure.
The description will be more fully understood with reference to the following figures, which are presented as exemplary embodiments of the invention and should not be construed as a complete recitation of the scope of the invention, wherein:
Turning now to the drawings, novel three-dimensional molecular clusters and methods of their synthesis are provided. In many embodiments the three-dimensional molecular clusters are perfunctionalized polyhedral boranes and carboranes. In some such embodiments the polyhedral boranes and carboranes are dodecaborates. In still other embodiments methods for synthesizing and perfunctionalizing such three-dimensional clusters are also provided.
In various embodiments, the three-dimensional clusters are configured to manipulate the photophysical properties of other materials, including, for example, for use as photooxidants or as components in organic light-emitting diode materials. In other such embodiments the three-dimensional clusters may be formed as two-dimensional sheets of such clusters.
Various other embodiments are directed to methods of forming atomically precise nanoparticles from such three-dimensional clusters, and to atomically precise molecular scaffolds formed from such three-dimensional clusters. In embodiments the atomically precise nanoparticles are formed by appending perfluoroaryls thereto followed by functionalizing the fluoroaryls with thiol-containing molecules and macromolecules. In various such embodiments the atomically precise nanomolecules may be utilized in a variety of organomimetic applications. In some such embodiments the biomimetic nanomolecules may be used with glycoconjugates that are linked with one or more molecules selected from the group consisting of proteins, peptides, lipid and saccharides. In other such embodiments the molecular scaffold forms an organomimetic cluster nanomolecule that functions as one of an antibody, protein, histone or viral mimic. In still yet other such embodiments the molecular scaffold operates as a viral assay.
These and other methods, materials and applications of said methods and materials will be described in greater detail in the disclosure.
Design and Synthesis of Three-Dimensional Molecular Clusters
Macromolecules in living systems usually act in tandem by constantly binding and interacting with each other. (See, e.g., Keskin, O. et al., Chem. Rev. 2008, 108, 1225-1244, the disclosure of which is incorporated herein by reference.) These protein-protein (PPIs) or protein-oligonucleotide interactions are known to mediate a large number of essential regulatory and assembly processes. Furthermore, viruses and bacteria capitalize on complex machinery consisting of several protein-protein interactions in order to penetrate and infect the host cell. Rationally designing and constructing abiotic systems that can interact precisely with large biomolecules remains a largely unsolved challenge given the molecular complexity of many PPIs and the large surface areas of these interactions. (See, e.g., Peczuh, M. W.; Hamilton, A. D. Chem. Rev. 2000, 100, 2479-2494; Wilson, A. J. Chem. Soc. Rev. 2009, 38, 3289-3300; Azzarito, V., et al., Nature. Chem. 2013, 161-173; Echols, H., Science 1986, 233, 1050-1056; Arkin, M. R.; Wells, J. A., Nat. Rev., Drug Disc. 2004, 3, 301-317; Jain, R. K.; Hamilton, A. D., Org. Lett. 2000, 2, 1721-1723; Park, H. S., et al., Proc. Natl. Acad. Sci. U.S.A 2002, 99, 5105-5109; Leung, D. K., et al., Proc. Natl. Acad. Sci. U.S.A 2000, 97, 5050-5053; and Rodriguez, J. M., et al., ChemBioChem 2009, 10, 829-833, the disclosures of each of which are incorporated herein by reference.) Because these interactions usually occupy such large surfaces (ranging from 500 to 4000 Å2/molecule), any general solution to designing PPI inhibitors will require molecules with relatively large surface areas as well.
The current toolbox of available molecules consists primarily of only two distinct structural classes—small molecules (
The advent of nanotechnology has recently provided researchers with ways to create a new class of hybrid nanoparticles, which can feature large surface footprints and essentially unlimited number of possible building block constituents (
Tremendous advances have been made by researchers in chemistry and engineering over the past decade exploring fundamental properties of these nanoparticle assemblies and the associated applications including those in delivery, sensing, diagnostics and “materials by design” technologies. However, all of these systems suffer from several fundamental limitations. Unlike proteins and small-molecules, hybrid nanoparticle assemblies are never atomically precise and therefore have non-uniform composition and size (
Embodiments are now provided that take advantage of inorganic chemistry to develop a wide-array of cluster-based scaffolds (as shown for example in
Many embodiments are directed to methods for synthesizing atomically precise cluster nanomolecules that can perform as three-dimensional scaffold. The ideal platform for nanoparticle synthesis should incorporate several key design elements including: a) functional group tolerance, b) modularity and c) robustness. Furthermore, given that nanoparticle scaffolds classically exhibit a large degree of rigidity the chemistry should allow for producing similarly rigid and semi-rigid scaffolds. Accordingly, embodiments are fundamentally different from the majority of existing classes of dendrimers, which are significantly more flexible and therefore less topologically structured. (See, Fréchet, J. M. J., Proc. Natl. Acad. Sci. 2002, 99, 4782-4787; Moore, J. S., Acc. Chem. Res. 1997, 30, 402-413; and Mammen, M., et al., Angew. Chem., Int. Ed. 1998, 37, 2754-2794, the disclosures of which are incorporated herein by reference.)
Rapid Synthesis of B12 Clusters
There exist several relatively robust cluster species, which could be utilized as fundamental building blocks, unfortunately the majority of these species feature metal-containing vertices, which could potentially diminish the stability of the resultant hybrid constructs due to the necessity of forming metal-ligand bonds. (See, Zhu, M., et al., J. Am. Chem. Soc. 2008, 130, 1138; Peymann, T., et al., J. Am. Chem. Soc. 2001, 123, 2182-2185; Pope, T. M. and Müller, A. Polyoxometalate Chemistry: From Topology via Self-Assembly to Applications. Kluwer: 2001; and Zhu, Y., et al., Angew. Chem., Int. Ed. 2010, 49, 1295-1298, the disclosures of which are incorporated herein by reference.) A notable exception from these species are boron-rich clusters, which have been known to exhibit excellent stability both in the free form and with functional organic linkers appended to these species. (See, e.g., Muetterties, E. A. Boron Hydride Chemistry. Academic Press, 1975; Kaim, W., et al., Angew. Chem., Int. Ed. 2009, 48, 5082-5091; Ivanov, S. V., et al., J. Am. Chem. Soc. 2003, 125, 4694-4695; Li, T., et al., J. Am. Chem. Soc. 2005, 127, 17832-17841; Maderna, A., et al., Angew. Chem., Int. Ed. 2001, 40, 1661-1664; and Goswami, L. N., et al., Inorg. Chem. 2013, 52, 1701-1709, the disclosures of which are incorporated herein by reference.) Accordingly, many embodiments are directed to polyhedral boron-based scaffolds, such as B12 scaffolds.
The existence of an icosahedral dodecaborate [B12H12] cluster was first predicted by Lipscomb and co-workers in 1954. (See, e.g., B. C. Jr. W. H. Eberhardt and W. N. Lipscomb, J. Chem. Phys., 1954, 22, 989-1001, the disclosure of which is incorporated herein by reference.) In a subsequent theoretical molecular orbital-based approach published in 1955, Longuet-Higgins and Roberts predicted that such a cluster would only be stable as dianionic [B12H12]2-. (See, e.g., H. C. Longuet-Higgins and M. de V. Roberts, Proc. R. Soc. London, Ser. A, 1955, 230, 110-119, the disclosure of which is incorporated herein by reference.) A 1959 study by Shapiro and Williams suggested the possible formation of a [B12H12]2− icosahedron, and in 1960 this cluster was first successfully isolated and characterized as a triethylammonium salt by Pitochelli and Hawthorne, albeit in a relatively low yield. (See, e.g., I. Shapiro and R. E. Williams, J. Am. Chem. Soc., 1959, 81, 4787-4790; and A. R. Pitochelli and F. M. Hawthorne, J. Am. Chem. Soc., 1960, 82, 3228-3229, the disclosures of which are incorporated herein by reference.) Subsequent pioneering studies by Hawthorne, Knoth, Muetterties, and others initiated a new era in the field of boron cluster chemistry.
(See, e.g., E. B. Moore, L. L. Lohr and W. N. Lipscomb, J. Chem. Phys., 1961, 35, 1329; R. Hoffmann and W. N. Lipscomb, J. Chem. Phys., 1962, 36, 2179; R. Hoffmann and W. N. Lipscomb, J. Chem. Phys., 1962, 37, 520; E. L. Muetterties, et al., J. Am. Chem. Soc., 1962, 84, 2506-2508; R. Hoffmann and W. N. Lipscomb, J. Chem. Phys., 1962, 37, 2872; H. C. Miller, et al, J. Am. Chem. Soc., 1963, 85, 3885-3886; I. A. Ellis, et al., J. Am. Chem. Soc., 1963, 85, 3885-3885; E. L. Muetterties, et al., Inorg. Chem., 1964, 3, 444-451; W. R. Hertler, Inorg. Chem., 1964, 3, 1195-1196; W. R. Hertler and M. S. Raasch, J. Am. Chem. Soc., 1964, 86, 3661-3668; H. C. Miller, N. E. Miller and E. L. Muetterties, Inorg. Chem., 1964, 3, 1456-1463; W. H. Knoth, et al., Inorg. Chem., 1964, 3, 159-167; R. J. Wiersema and R. L. Middaugh, Inorg. Chem., 1969, 8, 2074-2079; J. A. Wunderlich and W. N. Lipscomb, J. Am. Chem. Soc., 1960, 82, 4427-4428; I. B. Sivaev, et al., Collect. Czech. Chem. Commun., 2002, 67, 679-727; M. Davidson, Royal Society of Chemistry, 2000, vol. 253; N. S. Hosmane, Boron Science: New Technologies and Applications, Taylor & Francis, 2011; C. Knapp, in Comprehensive Inorganic Chemistry II, Elsevier, 2013, pp. 651-679; D. Olid, et al., Chem. Soc. Rev., 2013, 42, 3318; V. Geis, et al., Dalton Trans., 2009, 2687, the disclosures of which are incorporated herein by reference.) Specifically, these groups have shown that [B12H12]2− can be prepared on a large scale in a high yield (>90%) and undergo facile functionalization chemistry that parallels some properties of classical organic molecules (e.g. benzene). This was an exciting discovery, since previously many boron hydride clusters were perceived as highly unstable species prone to fast degradation by heat, acids, and bases. Conversely, [B12H12]2− salts were shown to be stable in acids and bases, and were thermally stable as high as 810° C. with no observable decomposition, see
Knoth and coworkers were the first to demonstrate the persubstitution of [B12H12]2-, producing halogenated [B12F12]2-, [B12Cl12]2-, [B12Br12]2− and [B12I12]2− derivatives. (See, e.g., W. H. Knoth, et al., J. Am. Chem. Soc., 1962, 84, 1056-1057, the disclosure of which is incorporated herein by reference.) In the past two decades, persubstitution of [B12H12]2− was improved with new synthetic methods and extended towards other functional groups including [B12Me12]2− and [B12(OH)12]2-. (See, e.g., W. Gu and O. V. Ozerov, Inorg. Chem., 2011, 50, 2726-2728; D. V. Peryshkov, et al., J. Am. Chem. Soc., 2009, 131, 18393-18403; S. V. Ivanov, et al., J. Am. Chem. Soc., 2003, 125, 4694-4695; M. F. Hawthorne, Pure Appl. Chem., 2003, 75, 1157-1164; T. Peymann, et al., Angew. Chem., Int. Ed., 1999, 38, 1061-1064, the disclosures of which are incorporated herein by reference.) Among the perfunctionalized derivatives synthesized, closo-[B12(OH)12]2− is particularly appealing, as it is capable of undergoing further functionalization by forming ether, ester, carbonate, and carbamate linkages. (See, e.g., O. K. Farha et al., J Am. Chem. Soc., 2005, 127, 18243-18251, the disclosure of which is incorporated herein by reference.)
While controlled oxidation of the parent [B12H12]2− anion leads to an irreversible cluster degradation forming a B—B linked dimer, several perfunctionalized variants have been previously observed to undergo reversible redox behavior. (See, e.g., W. Kaim, et al., Angew. Chem., Int. Ed., 2009, 48, 5082-5091, the disclosure of which is incorporated herein by reference.) For example, Rupich reported that [B12X12]2− could undergo a single electron oxidation to form a stable radical [B12X12]1-, which was recently isolated and structurally confirmed as the oxidized radical [B12Cl12]1-species by Knapp and coworkers. (See, e.g., M. W. Rupich, J. Electrochem. Soc., 1985, 132, 119; and R. T. Boeré, et al., Angew. Chem., Mt. Ed., 2011, 50, 549-552, the disclosures of which are incorporated herein by reference.) Hawthorne and co-workers reported that the perfunctionalized [B12(OCH2Ph)12] cluster can exist in three distinct redox states accessible via two sequential and quasi-reversible one-electron oxidation reactions of the parent dianionic closo species. (See, e.g., T. Peymann, et al., Angew. Chem., Int. Ed., 2001, 40, 1664-1667, the disclosure of which is incorporated herein by reference.) The same group later showed that other benzyl and alkyl functionalized B12(OR)12 clusters can be synthesized, and all of these species exhibit similarly reversible redox behavior. Schleid and co-workers subsequently showed that the parent [B12(OH)12]2− cluster can undergo a one-electron oxidation to form a stable radical [B12(OH)12]1− species. (See, e.g., N. Van, et al., Chem. — Eur. J., 2010, 16, 11242-11245, the disclosure of which is incorporated herein by reference.) Interestingly, the redox potential of the ether-linked B12(OR)12 species can be rationally tuned as a function of the 0-bound substituent, reminiscent of many metal-based redox-active inorganic complexes. (See, e.g., M. W. Lee, et al., Angew. Chem., Mt. Ed., 2007, 46, 3018-3022, the disclosure of which is incorporated herein by reference.) Unfortunately, all of the reported synthetic routes towards B12(OR)12 clusters currently require either extremely long reaction times (weeks) or highly specialized high pressure equipment. Furthermore, in all cases strict inert atmospheric conditions are also required for their synthesis.
Embodiments are directed to a rapid, scalable, and robust synthetic route to a wide range of perfunctionalized B12(OR)12 cluster derivatives. Various embodiments provide a microwave-based method that enables synthesis of perfunctionalized ether-linked boron clusters within minutes and does not require the use of inert atmosphere and rigorously dried solvents. In addition, embodiments of the methods may be used to prepare previously unknown B12(OR)12 derivatives featuring highly oxidizing redox potentials as well as vertex differentiated molecular architectures. Using embodiments of such methods allow for the full realization of the clusters' superior chemical and thermal inertness, relatively low cost compared to other polyhedral boron clusters, and isolation and characterization of a significant number of alkoxy-based derivatives, showing how one can rationally tune the relative redox and photophysical properties of the (−2) to (−1) to (0) species simply by varying the electronic properties of the substituent group (R) that is attached to the oxygen site of B12(OR)12, as shown schematically in
Various embodiments operate through the functionalization of the B—OH vertices with a diverse range of moieties, as shown schematically in
In accordance with many embodiments, methods for the perfunctionalization of boron-rich clusters allowing one to efficiently graft molecules around these cores are provided. As shown in
Various embodiments utilize the tetrabutylammonium (TBA) salt of closo[B12(OH)12]2− (TBA2[1]) was chosen for use with our microwave synthesis due to its enhanced solubility in organic solvents compared to alkali metal salts of [1] (
Other embodiments optimize the microwave reaction times with allyl bromide and bromoethane reagents independently, and in both cases demonstrate that complete substitution can be accomplished within 15-30 minutes at 140° C. These compounds were isolated in their fully oxidized neutral form in a similar fashion to [2]0, (compounds [3]0 and [4]0, respectively;
The relatively short perfunctionalization reaction times made possible by the microwave technique in accordance with embodiments allows for the rate of product formation to outcompete the rate of degradation stemming from the presence of adventitious air and moisture during the synthesis. Accordingly, in various embodiments, the synthesis of [2] was conducted using as-received non-dried acetonitrile with the reagents added to a reaction vessel open to air. The open-air synthesis of [2] proceeded with full conversion in 15 minutes as indicated by 11B NMR spectroscopy on the crude mixture. Following the normal work-up procedure, [2]0 was isolated in a 63% yield, suggesting that rigorous exclusion of air and moisture is not necessary for this transformation using the methods according to embodiments. This open-air synthesis method was successfully used for all subsequent ether-based cluster syntheses reported.
Other embodiments explore the scope of this transformation by using longer-chain alkyl substituents. Hexyl chain substitution required increased reaction times compared to the shorter ethyl substituent, yet persubstitution was still achieved within two hours, as opposed to 8 hours when using a high-pressure reactor in accordance with the prior art (isolated as [5]0,
Based on the success of synthesizing long-chain olefin-containing moieties in accordance with embodiment, the compatibility of embodiments with less stable reagents was investigated using ethyl 4-bromobutyrate with TBA2 [1]. Perfunctionalization with ethyl butyrate has been challenging using prior synthetic methods, requiring multiple step sequential additions of the alkyl halide and Hünig's base for 20 days while being handled under inert atmosphere conditions. (See, e.g., A. Pushechnikov, S. S. Jalisatgi and M. F. Hawthorne, Chem. Commun., 2013, 49, 3579-358, the disclosure of which is incorporated herein by reference.) However, utilizing microwave-assisted synthesis according to embodiments, the same product (
In various other embodiments the accessible electrochemical window for this class of compounds can be extended by utilizing benzyl halide precursors containing highly electron-withdrawing substituents. The perfunctionalized cluster featuring a trifluoromethyl (CF3) group attached to the para position of the benzyl moiety was prepared using our method in 30 minutes, and following oxidation the isolated neutral compound [11]0 was obtained in 66% yield (
For example, according to the trend suggested by this Hammett plot, a para-nitrobenzyl-substituted cluster should exhibit a higher 1−/0 oxidation potential than [11] (
Using embodiments of the microwave method described above, cluster [13] was synthesized in 30 minutes. Unlike all of the synthesized clusters reported thus far, the post-microwave reaction mixture was colorless, which is a characteristic feature of the pure dianionic state [13]2− for these clusters. The lack of color persisted even after column chromatography purification on silica gel in air. The identity of the pure isolated TBA salt of [13]2− (73% yield) was validated by full spectroscopic characterization and mass spectrometry. Oxidation of [13]2− with FeCl3.6H2O did not produce the neutral cluster, rather the pure [13]1− radical species was isolated in 78% yield, resulting in 56% net yield for [13]1− species starting from TBA2[1]. Use of stronger chemical oxidants such as ceric ammonium nitrate (CAN) degraded the boron cage, producing a diagnostic 11B NMR resonance at δ 20 characteristic of borates. (See, e.g., C. G. Salentine, Inorg. Chem., 1983, 22, 3920-3924, the disclosure of which is incorporated herein by reference.) Nevertheless, using embodiments of the method neutral cluster [13]0 was observed electrochemically via infrared spectroelectrochemistry (IR-SEC) and cyclic voltammetry (CV) in CH2Cl2 (
The structural parameters of the boron clusters featuring persubstituted vertices can exhibit significant distortions in the solid state as a function of the substituent and the redox state as determined by X-ray crystallographic studies. Specifically, [2]2− exhibits nearly identical B—B bond distances (1.781(4)-1.824(4) Å) and angles (B—B—B 107.798°<a<109.229°) as expected for a perfect icosahedron, yet as the cluster is oxidized to the electron-deficient [2]1− the structure expands and distorts slightly, with further distortion observed in the neutral state. Additionally, the B—O bond lengths decrease as the cluster is oxidized from [2]2-, which contains the longest average B—O distances, to the neutral [2]0 state with the shortest B—O distances. This observed trend of B—B bond lengthening, B—O bond contraction, and B—B—B angle distortion within the core as a function of cluster oxidation state is supported qualitatively by the crystal structures for neutral [11]0 and radical [13]1− (
X-ray photoelectron spectroscopy (XPS) has been widely used to study oxidation states in inorganic compounds. (See, e.g., N. V. Alov, J. Anal. Chem., 2005, 60, 431-435; W. Temesghen and P. Sherwood, Anal. Bioanal. Chem., 2002, 373, 601-608; X. P. Zhu, et al., Appl. Surf Sci., 2006, 252, 5776-5782; and M.-Y. Xing, et al., J. Phys. Chem. C, 2011, 115, 7858-7865, the disclosures of which are incorporated herein by reference.) This technique can therefore be utilized to further elucidate the oxidation state and effect of functionalization for the boron clusters according to embodiments. Boron XPS spectra for several representative clusters synthesized in (
In addition to previously mentioned benefits such as shortened reaction durations and the lack of stringent requirements for inert reaction conditions, microwave-assisted synthesis according to embodiments allows for one-pot, single-step reactions that would otherwise require more elaborate protocols. Mono-substitution of a benzyl ligand followed by persubstitution of the remaining eleven vertices has previously required a lengthy process involving several steps, whereas methods according to embodiments demonstrate a one-pot approach enabled by the described microwave-based method. (See, e.g., L. N. Goswami, et al., J. Org. Chem., 2012, 77, 11333-11338, the disclosure of which is incorporated herein by reference.)
For example, mixed-substituent B12(OEt)11(OBn) cluster ([14],
In summary, embodiments are directed to a rapid microwave-assisted synthetic route to perfunctionalized ether-linked B12(OR)12 clusters is disclosed and the robust nature of the technique demonstrated by the synthesis and characterization of multiple derivatives of [1]. For previously synthesized compounds, reaction duration was significantly reduced and prior requirements for oxygen-free and anhydrous reaction conditions were eliminated. Embodiments of the method also allow for a unique one-pot synthesis of mixed-substituent clusters with good selectivity under the same open-air conditions. The cluster species described here maintain the attractive properties of earlier derivatives, behaving as redox-active cores that show delocalization of electrons throughout the entire 3D boron cage, while the new functional groups provide a significant expansion to the available tuneable redox potential window for this class of clusters.
Palladium Cross-Coupling of B-Bromo-Carboranes
As described previously, carboranes are boron-rich molecules that can be functionalized through metal-catalyzed cross coupling. Many embodiments are directed to the use of bromo-carboranes in palladium-catalyzed cross-coupling for efficient B—N, B—O, and unprecedented B—CN bond formation. It is observed that in many cases bromo-carboranes outperform the traditionally utilized iodo-carborane species. This marked difference in reactivity can be leveraged in embodiments to circumvent multistep functionalization by directly coupling small nucleophiles (—OH, —NH2, and —CN) and multiple functional groups onto the boron-rich clusters.
Icosahedral carboranes are boron-rich molecular clusters that are often described as three-dimensional (3D) analogs to benzene. As previously discussed, their unique delocalized 3D aromatic bonding, high stability, and potential for site-selective functionalization make them attractive building blocks for tunable pharmacophores, unique ligand scaffolds, and building blocks for materials applications. Further development of these and other applications with carboranes requires efficient methods for cluster synthesis and functionalization, where ultimately each individual vertex can be specifically addressed.
Over the past 50 years, palladium-catalyzed cross-coupling has emerged as a powerful synthetic method for creating new molecules. (See, e.g., de Meijere, A.; Diederich, F. Metal-catalyzed Cross-coupling Reactions, 2nd ed.; Wiley-VCH: Weinheim, 2008, the disclosure of which is incorporated herein by reference.) In particular, the emergence of designer ligands (beyond PPh3) for Pd-catalyzed cross-coupling dramatically expanded the scope of electrophile substrates beyond aryl iodides. (See, e.g., Jacobsen, E. N. Adv. Synth. Catal. 2015, 357, 2173, the disclosure of which is incorporated herein by reference.) These new catalyst systems demonstrated a clear ability to cross-couple aryl-bromides and aryl-chlorides, thereby facilitating transformations of synthetically challenging substrates. Among existing ligand platforms, biaryl phosphine ligands significantly increased the efficacy of Pd-catalyzed C—C, C—N, and C—O bond formation. (See, e.g., Surry, D. S.; Buchwald, S. L. Angew. Chem., Int. Ed. 2008, 47, 6338, the disclosure of which is incorporated herein by reference.)
Despite these advances in catalyst design for aromatic substrates, effective methodologies for metal-catalyzed B—N, B—O and B—C cross-coupling in carboranes are lacking. In fact, only B-iodo-carboranes have been used in Pd-catalyzed cross-coupling thus far. (See, e.g., Zakharkin, L. I. et al., J. Organomet. Chem. 1982, 226, 217; Li, J., et al., Inorg. Chem. 1991, 30, 4866; Zheng, Z., et al., Inorg. Chem. 1995, 34, 2095; Jiang, W., et al., Inorg. Chem. 1995, 34, 3491; Villas, C, et al., Inorg. Chem. 2001, 40, 6555; Mukhin, S. N., et al., Organometallics 2008, 27, 5937; Sevryugina, Y., et al., Inorg. Chem. 2010, 49, 10627; Olid, D., et al., Chem. Soc. Rev. 2013, 42, 3318; Qui, Z. Tetrahedron Lett. 2015, 56, 963; Kracke, G. N., et al., ChemMedChem 2015, 10, 62, the disclosures of which are incorporated herein by reference.) Embodiments are directed to B-functionalized electrophiles, beyond B-iodo-carboranes, which may be competent cross-coupling partners, and demonstrating for the first time that B-bromo-carboranes can be efficient electrophiles for B—N, B—O, and B—CN bond formation in Pd-catalyzed cross coupling. Furthermore, conditions are provided where these B-bromo-carboranes are superior to the iodinated congeners enabling the synthesis of previously inaccessible B-substituted carboranes. This chemistry is furthermore attractive given the greater synthetic accessibility of B-bromo-carboranes compared to their iodo-based congeners.
Hawthorne and co-workers recently reported Pd-catalyzed amidation of 9-I-m-carborane (I-mCB) utilizing the biaryl phosphine ligand DavePhos (L1,
This example demonstrates the potential competence of BrmCB toward cross-coupling (
To further probe the scope of B—N bond formation using Br-mCB, we evaluated several conditions and substrates for Pd-catalyzed amination. Using morpholine as a substrate ([2a],
In general, cross-coupling using unprotected nitrogen-rich heterocyclic substrates is known to be challenging. (See, e.g., Mem M. A., et al., J. Am. Chem. Soc. 2013, 135, 12877, the disclosure of which is incorporated herein by reference.) Amination of halocarboranes has only been shown on the 2-I-p-carborane, which is a significantly more reactive substrate than Br-mCB. (See, e.g., Beletskaya, et al., Organometallics 2007, 26, 2340, the disclosure of which is incorporated herein by reference.) Embodiments of the cross-coupling methodology addresses this issue for the first time in the context of m-carborane chemistry since [2e] represents the first product resulting from the direct cross-coupling of an unprotected five-membered heterocycle with a B-halo-m carborane.
The versatility of Br-mCB as a cross-coupling partner can be further seen from its efficient reaction with challenging nucleophiles. For example, Br-mCB cross-couples with ammonia producing [2c] (
It can be observed that B—OH coupling with Br-mCB ([2f]) when nonanhydrous bases were used. This is remarkable, given that the only example of a Pd-catalyzed carborane B—O bond formation was reported on 2-I-p-carborane. Importantly, the I-mCB congener was previously deemed too unreactive. (See, e.g., Kabytaev, K. Z., et al., Organometallics 2009, 28, 4758, the disclosure of which is incorporated herein by reference.) Embodiments of methods provide a cross-coupling protocol enabling the direct coupling of water, methanol, trifluoroethanol, and 3,5-dimethylphenol with BrmCB ([2f-2i],
This constitutes a novel Pd-catalyzed cross-coupling leading to a B—O bond formation with m-carborane substrates. Significantly, a control reaction where I-mCB was used as a substrate led to a significantly lower conversion to [2i] (
The versatility of embodiments of the Br-mCB cross-coupling with small nucleophiles also allows for the activation of B—CN bond formation. Cyanide is known to be a difficult cross-coupling partner in metal catalysis due to its propensity toward binding to catalytically active species, resulting in their deactivation. (See, e.g., Sundermeier, M., et al., Chem.-Eur. J. 2003, 9, 1828; Schareina, T., et al., J. Organomet. Chem. 2004, 689, 4576; Erhardt, S., et al., J. Am. Chem. Soc. 2008, 130, 4828; and Senecal, T. D., et al., Angew. Chem., Int. Ed. 2013, 52, 10035, the disclosures of which are incorporated herein by reference.) Recently several groups reported efficient protocols for cyanation of aromatic substrates using K4[Fe(CN)6] as a mild cyanide source. (See above citations.) Pd-catalyzed cyanation of Br-mCB using K4[Fe(CN)6] with an L3-based precatalyst led to the formation of 9-CN-m-carborane in a nearly quantitive conversion ([3a],
The ability to append multiple functional groups is crucial to developing carboranes for new and existing materials. (See, e.g., Puga, A. V., et al., Chem. Commun. 2011, 47, 2252; Kabytaev, K. Z., et al., Eur. J. Inorg. Chem. 2013, 2013, 2488; Konieczka, S. Z., et al., Eur. J. Inorg. Chem. 2013, 2013, 134; Wright, J. H., et al., Inorg. Chem. 2013, 52, 6223; and Zhao, D., et al., Angew. Chem., Int. Ed. 2014, 53, 8488, the disclosures of which are incorporated herein by reference.) While polyfunctionalization of arene-based electrophiles via cross-coupling is well-established, similar methods for carboranes are rare. Embodiments of the current methodology can be applied toward di substitution cross-coupling chemistry. Specifically, 9,10-Br2-m-carborane [4a] can be functionalized with two bulky 3,5-dimethylphenolate substituents ([4c],
In addition, given the pronounced orthogonal reactivity of B—Br versus B—I bonds in cross-coupling, embodiments of the methodology can be used to heterofunctionalize mixed halo-carborane substrates. The selectivity of PdCl2(PPh3)2 can be leveraged for B—I bond functionalization to produce 9-Br-10-Et-m-carborane [4e] from 9-Br-10-I-m-carborane ([4b],
Selective Pd-catalyzed cross-coupling of the B—Br moiety in [4e] with L2-containing precatalyst yields the heterofunctionalized 9-O-(3,5-Me2C6H3)-10-Et-m-carborane [4f]. This transformation represents the first metal-catalyzed B-heterofunctionalization of di carba-closo-dodecaborane via cross-coupling demonstrating that B—Br-carboranes offer an additional pathway for multifunctionalization. These results also suggest that embodiments of the methodology are amenable to sterically encumbered carborane-based electrophiles.
Ortho-carboranes are the most challenging substrates in cross-coupling methodologies, since these species undergo facile deboronation in the presence of nucleophiles. (See, e.g., Fox, M. A.; Wade, K., J. Organomet. Chem. 1999, 573, 279, the disclosure of which is incorporated herein by reference.) Conditions used in embodiments are sufficiently mild and enable the cross-coupling of 3-Br-o-carborane (Br-o-CB) with amine and alcohol substrates that are not strongly nucleophilic ([5a-5b],
In summary, in accordance with embodiments B-bromo-m-carboranes undergo efficient Pd-catalyzed B—N, B—O, and B—CN cross-coupling enabled by precatalysts featuring electron-rich biaryl phosphine ligands. Although not to be bound by theory, the higher reactivity of Br-mCB likely stems from faster transmetalation (
3D Aromatic Boron-Rich Cluster Photooxidants
Many other embodiments are directed to perfunctionalized icosahedral dodecaborate clusters of the type B12(OCH2Ar)12 (Ar=Ph or C6F5) that can undergo photoexcitation with visible light, leading to a new class of metal-free photooxidants. In various embodiments, excitation in these species occurs as a result of the charge-transfer between low-lying orbitals located on the benzyl substituents and an unoccupied orbital delocalized throughout the boron cluster core. Some embodiments show how these species can participate in electron-transfer processes with a broad range of styrene derivatives, initiating their polymerization. Efficient initiation according to embodiments is observed in cases of both electron-rich and electron-deficient styrene monomers featuring para, meta and ortho-substituents at cluster loadings as low as 0.05 mol %. Furthermore, in some embodiments photo-excitation of B12(OCH2C6F5)12 in the presence of a less activated olefin such as isobutylene results in the production of highly branched poly(isobutylene). Accordingly, various embodiments are directed to a new class of air-stable metal-free photoredox reagents capable of mediating chemical transformations.
Photoredox processes are ubiquitous in chemistry and require a chromophore to absorb a photon, triggering the formation of a metastable state with a dramatically different redox potential than the parent ground state. Well-defined molecular chromophores typically possess functional groups that are capable of absorbing light, upon which an electron is promoted into a higher energy molecular orbital; in many of these cases, these photo-excited species can behave as photooxidants or photo-reductants. There exist two broad classes of molecular-based chromophores capable of undergoing photo-redox processes: metal-based complexes and organic dyes. (See, e.g., Prier, C. K., et al., Chem. Rev. 2013, 113, 5322-5363; Fagnoni, M., et al., Chem. Rev. 2007, 107, 2725-2756; and Narayanam, J. M. R.; Stephenson, C. R. J. Chem. Soc. Rev. 2011, 40, 102-113, the disclosures of which are incorporated herein by reference.) Metal-based chromophores possess excited states with highly tunable lifetimes, as they are able to reach triplet states and are also able to delocalize electrons over a number of molecular orbitals. (See, e.g., Kalyanasundaram, K. Coord. Chem. Rev. 1982, 46, 159-244; Fox, L. S., et al., Science, 1990, 247, 1069-1071; Juris, A., et al., Coord. Chem. Rev. 1988, 84, 85-277; Lumpkin, R. S., et al., J. Phys. Chem. 1990, 94, 239-243; Li, J., et al., Inorg. Chem., 2005, 44, 1713-1727, the disclosures of which are incorporated herein by reference.) On the other hand, the majority of organic chromophores possess relatively short-lived excited states featuring π→π* electronic excitations with radicals centered primarily within s or p orbitals. (See, e.g., Marin, M. L., et al., Chem. Rev. 2012, 112, 1710-1750, the disclosure of which is incorporated herein by reference.)(
A class of molecules that contain characteristics of both metal-complexes and organic molecules are boron-rich clusters. (See, e.g., Spokoyny, A. M. Pure Appl. Chem. 2013, 85, 903-919; and Mutterties, E. L., et al., Inorg. Chem. 1964, 3, 444-451, the disclosure of which are incorporated herein by reference.) As previously described, many polyhedral boron clusters are robust, kinetically stable, and can undergo facile functionalization chemistry. (See, e.g., Grimes, R. N. J. Chem. Ed 2004, 81, 657-672; Hawthorne, M. F. J. Chem. Ed. 2009, 86, 1131; Kaim, W., et al., Angew. Chem. Int. Ed 2009, 48, 5082-5091; Power, P. P. Chem. Rev. 2003, 103, 789-809; Aihara, J. J. Am. Chem. Soc. 1978, 100, 3339-3342; and King, R. B. Chem. Rev. 2001, 101, 1119-1152, the disclosures of which are incorporated herein by reference.) In particular, dodecaborate clusters feature a unique, 3D aromatic bonding situation in which the skeletal electrons are delocalized in three dimensions. (See, e.g., Lorenzen, V., et al., Inorg. Chem. 1998, 37, 4011-4014, the disclosure of which is incorporated herein by reference.) Importantly, in the context of photo-oxidation, unfunctionalized boron-rich clusters containing B—H bonds do not absorb light in the visible region and also cannot undergo well-defined redox processes. (See, e.g., Sivaev, I. B., et al., Collect. Czech. Chem. Commun. 2002, 67, 679-727; and Pitochelli, A. R. and Hawthorne, M. F. J. Am. Chem. Soc. 1960, 82, 3228-3229, the disclosures of which are incorporated herein by reference.) However, researchers previously demonstrated that several classes of perfunctionalized polyhedral boron clusters are capable of undergoing reversible redox processes. (See, e.g., King, B. T., et al., J. Am. Chem. Soc. 1996, 118, 10902-10903; Lee, M. W., et al., Angew. Chem. Int. Ed 2007, 46, 3018-3022; Peymann, T., et al., Angew. Chem. Int. Ed 2001, 40, 1664-1667; Maderna, A., et al., Angew. Chem. Int. Ed. 2001, 40, 1661-1664; Peymann, T., et al., Angew. Chem. Int. Ed. 1999, 38, 1061-1064; and Wixtrom, A. I., et al., Inorg. Chem. Frontiers 2016, the disclosure of which are incorporated herein by reference.) For example, colorless ether-functionalized [B12(OR)12]2− clusters can undergo two sequential quasi-reversible one-electron redox processes leading to [B12(OR)12]1− and neutral B12(OR)12, respectively, both of which exhibit strong visible light absorption bands (
Using embodiments of methods for perfunctionalizing B12(OR)12 clusters using microwave technology previously described it is possible to rationally tune the electrochemical properties of B12(OR)12 products using a variety of benzyl substituents (
According to embodiments, a similar process operates with the B12(OBn)12 system and clusters functionalized with more electron-withdrawing substituents increase the oxidation potential of the photo-initiator, thereby providing greater photo-oxidizing power of these species. Therefore, B12(OCH2C6F5)12 [1b] was synthesized in a manner analogous to that of [1a] and was isolated as a yellow solid in 63% yield (
In various embodiments, addition of 0.1 mol % [1b] to a 2M CH2Cl2 solution of [2a] under ambient lighting resulted in the instantaneous formation of a polymer gel featuring a high dispersity (
In order to understand the nature of the observed photo-initiation TD-DFT studies were performed on [1a] and [1b]. This work reveals the existence of a favorable LMCT-like (aryl-to-boron cluster) excitation pathway leading to an excited species with a redox potential roughly matching the oxidation potential of styrene species (
Photophysical measurements were then employed to probe the excited-state properties of [1b]. The excited-state lifetime of [1b], measured from the 600 nm emission maximum, was found to be on the order of ˜380 ps. From this data, in addition to the ground-state oxidation potential tabulated above, an excited-state oxidation potential value of ˜2.98 V was calculated for 1b. This value is consistent with the ability of [1b] to initiate the polymerization of [2a]. The photo-induced oxidative behavior of persubstituted clusters in accordance with embodiments is unprecedented and stands as a new contribution to the field of molecular photo-redox chemistry. Furthermore, the kinetic stability of both the neutral and monoanionic clusters due to the 3D delocalization of valence electrons within the cluster core provides a distinct strategic advantage for implementation in systems amenable to photochemistry involving a diversity of functional groups and reactive radical species. Notably, the polymerization of [2a] initiated by [1b] also proceeds under ambient conditions, affording a polymer of similar quality as that generated from a reaction set up under inert gas conditions. This is consistent with both a cationic mechanism of the observed process and the notion of the kinetic redox stability of these clusters (vide supra).
Given this successful polymerization, embodiments allow for the expansion of the substrate scope by employing styrene monomers [2b-2i], which possess a range of electronic and steric profiles. Polymerization of styrene [2b] with 0.1 mol % [1b] produced polystyrene in yields averaging 96% in 4 hours. Varying the catalyst loading did not have an effect on the molecular weight or dispersity of poly-2b.
Notably, the pyrilium-based catalyst utilized by Nicewicz does not produce polystyrene. However, in accordance with embodiments polymers of other electron-rich styrenes are generated in the presence of [1b] within hours in good yield (
The perfluorinated nature of [1b] poses the question of whether the successful polymerization of such a wide range of styrene monomers in comparison to either [1a] or [II] (
Accordingly, in accordance with embodiments and in light of the high excited-state oxidation potential (vide supra) of [1b], boron clusters are able to coax reactivity out of more challenging substrates. Typical cationic polymerization of isobutylene, a less activated than styrene, utilizes metal catalysts or harsh conditions. (See, e.g., Chen, M., et al., Chem. Rev. 2016, the disclosure of which is incorporated herein by reference.) A notable exception is the work of Michl and co-workers, who documented a Li+-catalyzed polymerization of isobutylene supported by a weakly-coordinated monoanionic carborane.
Irradiation (450 nm) of a 2M solution of [1b] in CH2Cl2 at pressures of isobutylene as low as 1 psi for 4 hours at room temperature in accordance with embodiments produced polymeric material. Neither irradiation of isobutylene in the absence of [1b] nor stirring [1b] in the presence of isobutylene in the dark, under otherwise identical reaction conditions as described above, afforded polymer. Interestingly, 1H and 13C NMR spectroscopy of the formed polymer material closely resembles the polymer obtained by Michl and is consistent with the formation of a highly branched poly(isobutylene) (
In conclusion, embodiments demonstrate—for first time—that icosahedral dodecaborate clusters of the type B12(OR)12, where R is a benzyl derivative, can undergo photoexcitation with visible light and activate styrene derivatives towards polymerization. Increasing the electron-withdrawing power of the benzyl substituents results in increased activity which allows for development of the first example of a visible-light photooxidant capable of polymerizing isobutylene. DFT calculations suggest that photoexcitation in these species occurs through the promotion of an electron from a low-lying, aryl-based orbital on the cluster substituent to an unoccupied cage-based orbital by visible (˜450 nm) light. Embodiments of B12-based clusters can behave as powerful yet air-stable redox-active chromophores that serve as highly reactive, metal-free alternatives to current systems for photoredox transformations. Embodiments also expand on an exciting untapped potential of molecular main-group systems as unique photoactive components.
Accordingly, in various embodiments, molecular chromophores and methods of their synthesis are provided. In many embodiments, the molecular chromophores are perfunctionalized icosahedral dodecaborate clusters. In various embodiments the clusters are of the type B12(OCH2Ar)12 (Ar=Ph or C6F5), which can undergo photo-excitation with visible light, leading to metal-free photooxidants. In embodiments, excitation in these species occurs as a result of the charge-transfer between low-lying orbitals located on the benzyl substituents and an unoccupied orbital delocalized throughout the boron cluster core. In various embodiments the air-stable metal-free photoredox reagents provided are capable of mediating chemical transformations. In many embodiments these species, when photo-excited (e.g., via an LED), participate in electron-transfer processes with a broad range of styrene derivatives, initiating polymerization. In many such embodiments, efficient initiation may be observed in cases of both electron-rich and electron-deficient styrene monomers featuring para, meta and ortho-substituents at cluster loadings as low as 0.05 mol %. In still other embodiments, photo-excitation of B12(OCH2C6F5)12 in the presence of a less activated olefin such as isobutylene results in the production of highly branched poly(isobutylene). In other embodiments the invention is directed to metal-free photooxidants comprising an icosahedral dodecaborate consisting of B12(OR)12 where R is a substituted aromatic.
In still other embodiments R is at least one of either a substituted or unsubstituted phenyl or C6F5. In yet other embodiments the invention is directed to a method for photo-mediated polymerization including, introducing a solution of a monomer and an icosahedral dodecaborate consisting of B12(OR)12 where R is a substituted aromatic; and illuminating the solution.
In still yet other embodiments R is at least one of either a substituted or unsubstituted phenyl or C6F5. In still yet other embodiments the monomer is a substituted or unsubstituted styrene. In some such embodiments the styrene is substituted with a functional group selected from the group of Me, Bu, F, and Cl.
Novel Complexes for Organic Light Emitting Diode Materials
Strong-Field Chelating Boron Cluster Ligands
Turning now to the drawings, organic light-emitting diode (OLED) materials with tunable properties featuring photophysically innocent boron-rich cluster ligands and methods of their synthesis are described. In many embodiments the materials and methods describe d8 metal complexes featuring robust and photophysically innocent strong-field chelating 1,1′-bis(ocarborane) (bc) ligand frameworks and methods of their synthesis. In various embodiments the dianionic bc ligand does not contribute to any visible metal-to-ligand charge transfer (MLCT) transitions, yet it provides strong ligand field in these complexes. Other embodiments are directed to a bc-based Pt(II) complex containing a 4,4′-di-tert-butyl-2,2′-bipyridine ligand (dtbbpy) that displays blue phosphorescent emission dominated by MLCT from the Pt(II) center to the bpy ligand. In some such embodiments the bulky three-dimensional nature of the be ligand precludes intermolecular Pt(II)•••Pt(II) interactions in the solid state where the resulting compounds retain their emission properties. Accordingly, embodiments are directed to designing organic light-emitting diode (OLED) materials with tunable properties featuring photophysically innocent boron-rich cluster ligands.
Many square planar platinum complexes containing chelating biaryl ligands have been established as efficient phosphorescent emitters, making them desirable dopants in organic light-emitting diodes (OLEDs). (See, e.g., H. Yersin, Ed. Highly Efficient OLEDs with Phosphorescent Materials; Wiley-VCH: Weinheim, 2008; P.-T. Chou and Y. Chi, Chem. Eur. J. 2007, 13, 380-395; Y. Chi, P.-T. Chou, Chem. Soc. Rev. 2010, 39, 638-655; J. Brooks, et al., Inorg. Chem. 2002, 41, 3055-3066; J. Kavitha, et al., Adv. Funct. Mater. 2005, 15, 223-229; S.-Y. Chang, et al., Inorg. Chem. 2006, 45, 137-146; S.-Y. Chang, et al., Dalton Trans, 2008, 6901-6911; Z. M. Hudson, et al., Adv. Funct. Mater. 2010, 20, 3426-3439; and X.-C. Hang, et al., Angew. Chem. Int. Ed., 2013, 52, 6753-6756, the disclosures of which are incorporated herein by reference.) The emissive properties of these Pt(II) complexes can be tuned by varying the electronic nature of the ligands surrounding the metal center; however, complete control over desired photophysical properties is still limited. For example, these square planar complexes are susceptible to aggregation as a consequence of the lack of steric bulk above and below the square plane, leading to intermolecular Pt(II)Pt(II) interactions that bring about luminescence quenching and red-shifting of the solid-state emission frequency. (See, e.g., D. Bandyopadhyay, et al., Inorg. Chem., 1983, 22, 1315-1321; L. Chassot, et al., Inorg. Chem. 1984, 23, 4249-4253; M. Ghedini, et al., Organometallics 1999, 18, 2116-2124; and K. E. Dungey, et al., Inorg. Chem. 2000, 39, 5192-5196, the disclosures of which are incorporated herein by reference.) Furthermore, in prototypical mixed ligand complexes, (L)(L′)Pt(II), the HOMO is generally both metal- and ligand-based (Pt(II) and L) while the LUMO is located on the remaining ligand (L′). (See, e.g., D. P. Rillema, et al., Inorg. Chem. 2013, 52, 596-607; and D. P. Rillema, et al., Dalton Trans. 2015, 44, 17075-17090, the disclosures of which are incorporated herein by reference.) This ultimately complicates the predictability of ligand effects on emission properties. A class of compounds that could kinetically stabilize the Pt(II) square planar framework without participating in electronic transitions would prove very useful for creating improved phosphorescent emitters for the next generation of OLED devices.
Icosahedral dicarba-closo-dodecaboranes (C2B10H12, carborane) are robust, charge neutral boron clusters that are often considered as 3D aromatic analogues to arenes. Unfunctionalized carborane species have an extremely large HOMO-LUMO gap (˜8 eV), making them potentially useful building blocks for probing their photophysical innocence in the context of metal-based phosphorescent emitters. (See, e.g., M. Scholz and E. Hey-Hawkins, E. Chem. Rev. 2011, 111, 7035-7062; and J. M. Oliva, et al., Phys. Chem. Chem. Phys. 2010, 12, 5101-5108, the disclosures of which are incorporated herein by reference.) Available functionalization routes through either carbon or boron vertices in these clusters also enable the synthesis of tailored ligand frameworks for transition metal complexes. (See, e.g., Y. Quan and Z. Xie, Angew. Chem. 2016, 128, 1317-1320; R. Cheng, et al., Angew. Chem. 2016, 128, 1783-1786; C. Tang and Z. Xie, Angew. Chem. Int. Ed. 2015, 54, 7662-7665; H. Lyu, et al., Angew. Chem. 2015, 127, 10769-10772. A. M. Spokoyny, Pure Appl. Chem. 2013, 85, 903-919; A. M. Spokoyny, et al., Organometallics 2012, 31, 8478-8481; C. A. Lugo, et al., Inorg. Chem. 2015, 54, 2094-2096; A. R. Popescu, et al., Coord. Chem. Rev. 2014, 269, 54-84; B. Xu, et al., Dalton Trans., 2015, 44, 1530-1533; J. Kahlert, et al., Dalton Trans. 2015, 44, 9766-9781; J. Li, et al., Inorg. Chem. 1991, 30, 4866-4868; Z. Zheng, et al., Inorg. Chem. 1995, 34, 2095-2100, the disclosures of which are incorporated herein by reference.) For example, it has been demonstrated that κ2-C,N-bound 1-(2-pyridyl)-o-carboranyl and κ2-C,P-bound 1-(iPr2PCH2)-o-carboranyl can be strong ancillary ligands that contribute to the electronic stabilization of bis(heteroleptic) Ir(III) species, leading to an arylpyridine-dominant phosphorescent emission. (See, e.g., H. J. Bae, et al., Dalton Trans. 2013, 42, 8549-8552; T. Kim, et al., Organometallics 2015, 34, 3455-3458; A. M. Prokhorov, et al., Chem. Commun. 2011, 47, 7713-7715; A. M. Prokhorov, et al., J. Am. Chem. Soc. 2014, 136, 9637-9642, the disclosures of which are incorporated herein by reference.)
From DFT calculations and analysis of the emission spectra, it has also been determined that the C-bound o-carboranyl unit remains uninvolved in electronic transitions and that phosphorescent emission results from MLCT of the Ir(III)-based HOMO to the arylpyridine-based LUMO. Furthermore, biaryl ligands have been functionalized with connected carboranyl moieties (ortho, meta, and para) to tune luminescent properties. (See, e.g., C. Shi, et al., Chem. Commun. 2013, 49, 4746-4748; C. Shi, et al., Angew. Chem. Int. Ed. 2013, 52, 13434-13438; T. Kim, et al., Inorg. Chem. 2013, 52, 160-168; H. J. Bae, et al., Inorg. Chem. 2014, 53, 128-138, the disclosures of which are incorporated herein by reference.) Despite these promising properties, a tunable, exclusively carborane-based ligand scaffold for phosphorescent emitter molecules has not been found. (See, e.g., X. Li, et al., Chem. Eur. J. 2015, 22, 1888-1898; and S. Mukherjee and P. Thilagar, Chem. Commun. 2016, 52, 1070-1093, the disclosures of which are incorporated herein by reference.) Such a ligand framework would be an ideal system for a rational design of metal-based luminescent complexes (vide supra).
In 1970, Hawthorne elegantly showed that the oxidative coupling of two o-carboranes [1] through carbon vertices yields 1,1′-bis(o-carborane) [2], effectively a 3D analogue of biphenyl (
Two monoanionic bidentate ligands are commonly used in Pt(II) architectures employed for OLEDs, but there are few examples of Pt(II)-based emitters containing a dianionic bidentate ligand and a neutral bidentate ligand. (See, e.g., C. Cornioley-Deuschel & A. von Zelewsky, Inorg. Chem. 1987, 26, 3354-3358; M. Maestri, et al., Helv. Chim. Acta 1988, 71, 1053-1059; C. B. Blanton, et al., Inorg. Chem. 1992, 31, 3230-3235; J. A. Zuleta, et al., J. Am. Chem. Soc. 1989, 111, 8916-8917; J. M. Bevilacqua & R. Eisenbery, Inorg. Chem. 1994, 33, 2913-2923; S. D. Cummings & R. Eisenberg, J. Am. Chem. Soc. 1996, 118, 1949-1960; W. Paw, et al., Coord. Chem. Rev. 1998, 171, 125-150; and M. Hissler, et al., Coord. Chem. Rev. 2000, 208, 115-137, the disclosures of which are incorporated herein by reference.) One such example is Pt(bph)(bpy)[12a-c] (where bph=biphenyl, bpy=2,2′-bipyridine). Embodiments employ bc in place of bph to introduce sufficient steric bulk above and below the square plane to eliminate intermolecular Pt(II)⋅⋅⋅Pt(II) interactions, which are often responsible for non-radiative decay pathways that lower luminescent efficiency. Additionally, the lack of an exposed π-aromatic system in embodiments comprising bc helps in reducing these undesirable intermolecular interactions and unwanted substitution and degradation pathways. Furthermore, the high-lying LUMO of embodiments incorporating bc should be inaccessible for orbital mixing and MLCT processes. Therefore, embodiments of the bc ligand provide kinetic stability while maintaining photophysical innocence in the context of designing OLEDs. Finally, emission originating from a single ligand according to embodiments yields greater color purity as mixing of emissions from multiple delocalized excited states will not be possible. Together, these properties allow for embodiments to rationally tune other ancillary ligands without electronic interference from bc.
The photophysical behavior of embodiments of be as a ligand has been evaluated in a series of d8 model transition metal complexes of the type M(bc)(dppe) (M=Ni(II), Pd(II), Pt(II); dppe=1,2-bis(diphenylphosphino)ethane;
To demonstrate that the bc framework according to embodiments is structurally similar to the biphenyl (bph) framework, bond distances, angles, and molecular geometries of [3a-3c] were compared to those of a series of cyclometallated M(bph)(L{circumflex over ( )}L) in reported X-ray crystal structures, and determined that bc does not influence the intramolecular geometry much differently than the bph ligand. Furthermore, the M-P bond lengths in [3a-3c] are also consistent with the strong-field ligand nature of bc in these complexes.
UV-Vis spectroscopic measurements performed on [3a-3c] revealed strong transitions in the UV region below 360 nm corresponding to π-π* transitions on the ligand. UV-Vis spectra of [3a-3c] also feature weaker intensity transitions in the visible region ranging from 400-500 nm that result from M(II)-(dppe) MLCT. DFT calculations performed on the geometry optimized X-ray crystal structure inputs of [3a-3c] confirm the nature of the observed electronic transitions. Computational studies reveal an almost entirely metal-based HOMO and dppe ligand-based LUMO with negligible contribution from the bc ligand in all frontier orbitals. Accordingly, bc chelated to the d8 transition metals in embodiments of complexes remains uninvolved in all MLCT-based visible transitions, suggesting its photophysical innocence in the UV-Vis region.
Other embodiments are directed to methods of synthesizing a Pt(II)-bpy (bpy=2,2′-bipyridine) complex chelated by bc, as Pt(II) complexes containing this class of ligands are known to exhibit phosphorescent emission. (See, e.g., C. Cornioley-Deuschel and A. von Zelewsky, Inorg. Chem., 1987, 26, 3354-3358; M. Maestri, et al., Helv. Chim. Acta, 1988, 71, 1053-1059; and C. B. Blanton, et al., Inorg. Chem., 1992, 31, 3230-3235, the disclosures of which are incorporated herein by reference.) Starting with the addition of Li2[bc] to a slurry of Pt(bpy)Cl2, a large amount of emissive, insoluble product was obtained. The extremely low solubility of this product in common organic solvents hampered its characterization. In order to potentially circumvent this issue, the 4,4′-di-tert-butyl-2,2′-bipyridine (dtb-bpy) ligand may be used as an alternative, anticipating more favorable solubility properties. Using the same synthetic route yielded, again, a largely insoluble, emissive solid (
A mixture of [4a] and [4b] was dissolved in hot 2-MeTHF and allowed to cool to room temperature, yielding single crystals of 4a (
Given that the bc framework according to embodiments is amenable to substitution, functionalizing this scaffold with alkyl groups may be used to increase the solubility of the resulting Pt(II) complexes, ultimately allowing for the better characterization of these emissive species. We therefore installed ethyl groups at the B(9) and B(12) positions of the parent 9,12-B-diiodo-o-carborane [5] using Kumada cross-coupling conditions producing bis(alkylated) species [6] (
Crystals of [8] suitable for X-ray analysis were grown by slow evaporation of diethyl ether over the course of one week. The diffraction study confirmed the presence of the asymmetric isomer with one Pt—C(1) bond and one Pt—B(4) bond (
Importantly, the intermolecular Pt(II) Pt(II) distances were augmented even more in the solid-state than in [4a] through the introduction of ethyl groups, yielding Pt(II)⋅⋅⋅Pt(II) distances of 5.891 Å (when ethyl groups face away from each other) and 7.979 Å (when ethyl groups point towards each other), effectively preventing any potential intermolecular Pt(II)⋅⋅⋅Pt(II) interactions (
Cyclic voltammetry (CV) of [8] reveals a reversible, one-electron reduction (E1/2Red=−1.92 V) and an irreversible one-electron oxidation (E1/2 Ox=0.85 V), as shown in Table 1 (below) and
Though electrochemical characterization for heteroleptic Pt(II) complexes bound by a dianionic bidentate ligand and neutral bidentate ligands are scarce, Table 1 presents redox potentials for two such examples, Pt(bph)(bpy) and Pt(bph)(en) (where en=1,2-ethylenediamine). (See, e.g., N. G. Connelly & W. E. Geiger, Chem. Rev., 1996, 96, 877-910, the disclosure of which is incorporated by reference.) The reduction potential for [8] is similar to the other two compounds (Table 1, Column 2); however, the oxidation potential of [8] is significantly greater (Table 1, Column 3). This is consistent with the strong field ligand character of the bc-based framework according to embodiments, which should make it more difficult to remove an electron from the Pt(II) HOMO level in [8].
Similar to [4a/4b], it is observed that [8] emits an intense blue-green color upon irradiation with a table-top UV lamp at 364 nm at room temperature. Given the improved solubility properties of [8] according to embodiments, it is possible to carry out a detailed series of photophysical measurements in order to ascertain the efficiency and nature of this luminescent behavior (
Similarly, the neat solid [8] also exhibits an emission profile with a resolved vibronic fine structure, further suggesting the ligand-centered emission. Compared to the emission profile from the neat solid, emission from the solution at 77 K is hypsochromically shifted by roughly 20 nm. This shift is expected as vibrational relaxations to a lower energy excited state will not be favorable at lower temperatures, resulting in a higher energy, blue-shifted emission observed for [8] at 77 K in 2-MeTHF. When [8] is doped in a PMMA matrix (2 wt. %), the emission profile is broadened and the peak is blue-shifted by about 8 nm versus the emission of the neat solid. The excited-state lifetime (t) for [8] increases as the environment becomes more rigid. This increase is significant, going from 0.94 μs as a neat solid, to 4.24 μs doped in PMMA, further to 11.4 μs at 77 K. This evidence suggests that decreasing vibrational motion through a more rigid and ordered surrounding environment in accordance with embodiments can preserve the excited state, possibly by minimizing the energy loss via non-radiative relaxation pathways.
From the measured excited state lifetimes and quantum yields for [8] doped in the PMMA matrix and neat solid in accordance with embodiments, the radiative rate constant (kr) and non-radiative rate constant (knr) could be calculated (Table 2). Though kr for the doped PMMA film is half that of the neat solid, knr for the doped PMMA film decreased by about a factor of 5, which supports the trend seen for measured τ values (vide supra). Additionally, the doped PMMA film according to embodiments exhibits a quantum yield (ϕ) more than twice that of the neat solid, as well as a lifetime that is about 4.5 times greater. Based on these data, it is likely that the PMMA film decreases access to a non-radiative decay pathway through its behavior as a rigid matrix.
The photophysical properties of [8] in accordance with embodiments, a DFT computational study was performed at the BP86-D3 level using the TZP basis set (
In general, phosphorescent blue OLEDs suffer from short lifetimes (˜600 hours) relative to their red and green counterparts (106 hours). Several groups have previously investigated the degradation of blue OLEDs and found that the decomposition of the phosphorescent dopant molecules occurs during regular use, greatly inhibiting the overall lifetime and efficiency of the device. (See, e.g., Y. Zhang, S. Lee and S. R. Forrest, Nat. Commun., 2014, 5, 1-7; S. Scholz, et al., Proc. SPIE, 2008, 69991B; V. Sivasubramaniam, et al., J. Fluorine Chem., 2009, 130, 640-649; I. R. de Moraes, et al., Org. Electron., 2011, 12, 341-347; and R. Seifert, et al., Org. Electron., 2013, 14, 115-123, the disclosures of which are incorporated herein by reference.) Thermogravimetric analysis of [8] suggests the bc ligand framework remains intact upon heating to 500° C. Accordingly, chelating boron cluster scaffolds according to embodiments may be used to ameliorate previously described stability issues in OLED devices.
In conclusion, compounds and methods for producing 1,1′-bis(-o-carborane) as a dianionic ligand (bc) in group 10 metal complexes are provided. From the synthesis and characterization of model complexes, it has been discovered that unlike the structurally reminiscent biphenyl ligand, (bc) displays a unique photophysical innocence and remains uninvolved in relevant photophysical transitions when bound to the group 10 transition metals. Furthermore, since bc introduces sufficient steric bulk above and below the square plane of the metal center, it effectively shuts down undesired intermolecular interactions in the solid-state. For Pt(II) complexes featuring phosphorescent emission properties, this unique ligand design aspect allows for the removal of any possible Pt(II)•••Pt(II) interactions, which commonly lead to luminescence quenching. Organomimetic properties of carboranes in general, and bc in particular, enable embodiments to rationally tune the processability of a blue phosphorescent emitting Pt(II) species. In other embodiments, the substitution of carborane-based ligands with bulkier functional groups can be used to minimize the excited state distortion. Some embodiments are directed to transition metal complex ligands comprising a 1,1′-bis(o-carborane) consisting of [(C2H10B10)−]2.
Other embodiments are directed to transition metal complex ligands comprising a substituted 1, 1′-bis(o-carborane) consisting of (C2H9B10R2)2, where R is selected from the group consisting of: alkane, alene, alkyne, alcohol, aryl, ether, halide, aldehyde, carboxylic acid, ester, amide, amine, nitrile, isocyanate, thiol and arene.
In still other embodiments the ligand is coordinated with a transition metal (M) at the CH group, and wherein the transition metal is selected from the group consisting of: Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ru, Rh, Pd, Ag, Re, Os, Ir, Pt and Au. In yet other embodiments the ligand is a bidentate ligand containing two N-M bonds. In some such embodiments the ligand is a monoanionic ligand containing one or either a C-M or B-M bond. In other such embodiments the monoanionic ligand is an acetylacetone. Still yet other embodiments are directed to transition metal complex carboranyl-aryl ligands consisting of C2H8B10R2X, where R is selected from the group consisting of: alkane, alene, alkyne, alcohol, aryl, ether, halide, aldehyde, carboxylic acid, ester, amide, amine, nitrile, isocyanate, thiol and arene; and where X is a substituted or unsubstituted aryl. In some such embodiments the aryl is a pyridine. These embodiments allow for a new avenue in designing luminescent materials with improved properties incorporating robust and photophysically innocent multidentate ligand platforms.
Zwitterionic Iridium (III) Complexes Featuring Nido-Carborane-Based Ligands
Various embodiments are directed to a new class of phosphorescent zwitterionic bis(heteroleptic) Ir(III) compounds containing pyridyl ligands with weakly coordinating nido-carboranyl substituents. Treatment of phenylpyridine-based Ir(III) precursors with C-substituted ortho-carboranylpyridines in 2-ethoxyethanol in accordance with embodiments results in a facile carborane deboronation and the formation of robust and highly luminescent metal complexes. The resulting nidocarboranyl fragments in accordance with embodiments associate with the cationic Ir(III) center through primarily electrostatic interactions. These compounds phosphoresce at blue wavelengths (450-470 nm) both in a poly(methylmethacrylate) (PMMA) matrix and in solution at 77 K. These complexes display structural stability at temperatures beyond 300° C. and quantum yields greater than 40%. Importantly, the observed quantum yields correspond to a dramatic 10-fold enhancement over the previously reported Ir(III) congeners featuring carboranyl-containing ligands in which the boron cluster is covalently attached to the metal. Embodiments are further directed to the use of a ligand framework containing a weakly coordinating anionic component to provide a new avenue for designing efficient Ir(III)-based phosphorescent emitters.
The past two decades have seen a surge in the development of fluorescent and phosphorescent emitters with ever-increasing efficiency and color purity. (For selected examples of blue OLEDs incorporating fluorescent emitters, see: Uoyama, H., et al., Adachi, C. Nature 2012, 492, 234; Méhes, G., et al., Angew. Chem., Int. Ed. 2012, 51, 11311; Lee, S. Y., et al., Angew. Chem., Int. Ed. 2014, 53, 6402; Kawasumi, K., et al., J. Am. Chem. Soc. 2015, 137, 11908; Zhang, Q., et al., Nat. Photonics 2014, 8, 326; Feuillastre, S., et al., J. Am Chem. Soc. 2016, 138, 3990; Li, K., et al., Chem. Commun. 2011, 47, 9075; and for selected examples of phosphorescent emitters for OLED applications, see: Yersin, H., Ed. Highly Efficient OLEDs with Phosphorescent Materials, Wiley-VCH: Weinheim, 2008; Chou, P.-T., et al., Chem. Soc. Rev. 2010, 39, 638; Lamansky, S., et al., J. Am. Chem. Soc. 2001, 123, 4304; Lamansky, S., et al., Inorg. Chem. 2001, 40, 1704; Tamayo, A. B., et al., J Am. Chem. Soc. 2003, 125, 7377; Sajoto, T., et al., Inorg. Chem. 2005, 44, 7992; Chang, C.-F., et al., Angew. Chem., Int. Ed. 2008, 47, 4542; Tsuboyama, A., et al., J. Am. Chem. Soc. 2003, 125, 12971; Maity, A., et al., Inorg. Chem. 2016, 55, 2299; Fleetham, T., et al., J. Org. Electron. 2012, 13, 1430; Turner, E., et al., J. Inorg. Chem. 2013, 52, 7344; Saris, P. J. G. & Thompson, M. E. Org. Lett. 2016, 18, 3960; Kui, S. C. F., et al., Chem. Commun. 2013, 49, 1497; Hudson, Z. M., et al., Adv. Funct. Mater. 2010, 20, 3426; and Ko, S.-B., et al., Dalton Trans. 2015, 44, 8433, the disclosures of each of which are incorporated herein by reference.) In particular, the continued development of efficient Ir(III)-based phosphorescent compounds, currently targeted for their potential use in organic light-emitting diodes (OLEDs) represents a vital component of this research. (See, e.g., Tremblay, J.-F. Chemical & Engineering News, Jul. 11, 2016; pp 30-34, the disclosure of which is incorporated herein by reference.) Previous work has shown that ligand choice is crucial for optimizing luminescence efficiencies, emission wavelengths, and emitter stability in these devices. Still, despite the significant progress that has been made so far, efficient and long-lasting blue phosphorescent emitters have remained largely elusive. (See, e.g., Zhang, Y., et al., Nat. Commun. 2014, 5, 5008; Fleetham, T., et al., J. Adv. Mater. 2014, 26, 7116; Lee, J., et al., Nat. Mater. 2015, 15, 92; Fleetham, T. B., et al., J. Chem. Mater. 2016, 28, 3276; Giebink, N. C., et al., J. Appl. Phys. 2008, 103, 044509; Seifert, R., et al., Org. Electron. 2013, 14, 115; and Holmes, R. J., et al., Appl. Phys. Lett. 2003, 82, 2422, the disclosures of which are incorporated herein by reference.)
The prevailing design principle for Ir(III)-based phosphorescent systems leverages covalently bound strong- and weak-field (chelating) donor ligands to deliver the desired properties of the luminescent species (
Carboranes, a class of icosahedral boron-based clusters recognized for their high stability and unique electronic properties, are used in embodiments as ligand components of emissive Pt(II)- and Ir(III)-based molecules toward implementation as dopants in OLEDs and as fluorophores in cell imaging. (Spokoyny, A. M.; et al., Nat. Chem. 2011, 3, 590; Grimes, R. N. Dalton Trans. 2015, 44, 5939; Tsang, M. Y., et al., Inorg. Chem. 2014, 53, 9284; Gabel, D. Pure Appl. Chem. 2015, 87, 173; Teixidor, F., et al., A. Chem.-Eur. J. 2015, 21, 12778; Kennedy, R. D., et al., Chem. Mater. 2013, 25, 3539; and Jiang, W., et al., Inorg. Chem. 2010, 49, 3252, the disclosures of which are incorporated herein by reference.) The distinctive electronic influence of carboranes, which behave as electron-withdrawing groups if bound through carbon and electron-releasing groups if bound through boron, provide a unique opportunity for isosteric electronic variation. Since complete control over vertex functionalization of carboranes is still a largely unsolved problem, researchers in the field of OLED development have employed more easily accessible C-functionalized carborane scaffolds to perturb the electronic manifold of metal-based phosphors. However, despite the electronic extremes accessible through carborane as a ligand, very few phosphorescent metal-based molecules have been developed that contain carborane directly bound to a metal center or that contain deboronated (e.g., nido) analogues; rather, carboranyl substituents are most commonly installed on the periphery of the ligand scaffolds where direct interaction of the metal and the carborane is not possible. (See, e.g., Bae, H. J., et al., Dalton Trans. 2013, 42, 8549; Kim, T., et al., Organometallics 2015, 34, 3455; Prokhorov, A. M., et al., Chem. Commun. 2011, 47, 7713; Prokhorov, A. M., et al., J. Am. Chem. Soc. 2014, 136, 9637; Shi, C., et al., Chem.-Eur. J. 2014, 20, 16550; Visbal, R., et al., J. Am. Chem. Soc. 2013, 135, 4712; Visbal, R., et al., Dalton Trans. 2014, 43, 328; Czerwieniec, R., et al., Inorg. Chem. 2010, 49, 3764; Crespo, O., et al., Inorg. Chem. 2003, 42, 2061; Crespo, O., et al., Chem.-Eur. J. 2014, 20, 3120; Shi, C., et al., Chem. Commun. 2013, 49, 4746; Kim, T., et al., Inorg. Chem. 2013, 52, 160; Shi, C., et al., Angew. Chem., Int. Ed. 2013, 52, 13434; Lee, Y. H., et al., J. Am. Chem. Soc. 2015, 137, 8018; Zhu, L., et al., Chem.-Eur. J. 2015, 21, 4721; Lee, Y. H., et al., Chem.-Eur. J. 2015, 21, 2052; Park, J., et al. Dalton Trans. 2016, 45, 5667; and Kim, Y. et al., Inorg. Chem. 2016, 55, 909, the disclosures of which are incorporated herein by reference.) As part of our ongoing studies of the organometallic chemistry of carboranes, we considered that deboronated carboranes, which are formally anionic, might be successfully employed as weakly coordinating/noncovalent ligands in building zwitterionic Ir(III)-based phosphorescent molecules.
We began our studies in pursuit of generating bis(heteroleptic) Ir(III) phosphors with a nido-carboranylpyridine ligand. A common tactic employed in designing metal-based phosphorescent molecules involves the installation of strong field ligands such as carbanions or N-heterocyclic carbenes to stabilize metal-based orbitals; it is also known, however, that the filled d-orbitals may also be stabilized if electron density is removed from the metal center, either as a consequence of electron-withdrawing ligands or if the metal center bears a formal positive charge. (See, e.g., Li, J., et al., Polyhedron 2004, 23, 419, the disclosure of which is incorporated herein by reference.) In both cases, the HOMO-LUMO gaps are widened, opening the possibility for blue-shifted, radiative excited-state decay. In accordance with embodiments, the dominant steric profile of the nido-carboranyl scaffold amidst an otherwise rigid octahedral metal environment minimizes metal-cage interactions such that the metal holds a greater proportion of the formal positive charge. In addition, the diffuse nature of the negatively charged nido-carboranyl substituent gives poor directionality for interaction with the metal, thereby maintaining the desired ionic/noncovalent interaction by restricting electron sharing with the Ir(III) center.
Embodiments of ligand [1a] were synthesized. The intermediate carboranylpyridine (
Treatment of Ir(F2ppy)2(acac) with [1a] under either microwave conditions or in an oil bath in 2-ethoxyethanol (EtOEtOH) for 3 h (
The solvent in this reaction was then removed in vacuo, and the resulting solid was subjected to additional spectroscopic characterization. The 1H NMR spectrum of the sample dissolved in CDCl3 showed diagnostic, upfield (˜−3.5 to −4.5 ppm) chemical shifts, characteristic of a hydride on the open face of a deboronated o-carborane. Precipitation of the Ir(III) species from hexanes afforded [2a] in 73% yield after purification. X-ray diffraction analysis of single crystals of the product [2a], grown from a concentrated EtOH solution at −15° C., confirmed the presence of the nido-carboranyl group (
In order to probe the effect of the nido-carboranyl ligand on the luminescent properties of Ir(III)-based compounds, several derivatives were synthesized featuring modified phenylpyridine (ppy) and carborane-based ligands. The deboronation of [1a] en route to formation of [2a] raises whether in embodiments it is necessary to protect the remaining carboranyl C—H vertex of [1b], particularly considering that C-functionalized o-carboranes containing electron-releasing substituents are generally more stable toward deboronation than the parent o-carborane were synthesized in an analogous manner to [2a] (
Embodiments of ligands, e.g., [2a-2d] are the first examples of luminescent iridium(III) compounds that employ a cyclometalated ligand which associates with the metal through weakly coordinating/noncovalent interactions, despite a large number of cationic, luminescent iridium complexes having been reported. Many of these cationic Ir(III) species exist as formal salts, while comparatively few zwitterionic species, which also contain formally cationic Ir(III) centers, have been documented. (See, e.g., Ladouceur, S. & Zysman-Colman, E. Eur. J. Inorg. Chem. 2013, 2013, 2985; Darmawan, N., et al., J. Mater. Chem. C 2014, 2, 2569; Byun, Y., et al., J. Appl. Phys. Lett. 2007, 91, 211106; Jiang, W., et al., Inorg. Chem. 2010, 49, 3252; and Li, J., et al., Polyhedron 2004, 23, 419, the disclosures of which are incorporated herein by reference.) In contrast to [2a-2d], the negatively charged component of these previously reported “inner-salt complexes” is distal to the metal center and the coordination environment around the Ir(III) center falls in line with the more traditional construct containing covalent metal-ligand bonds (
A suite of photophysical studies were carried out on embodiments [2a-2d] to evaluate the influence of the nido-carboranylpyridine ligand framework on the luminescent properties, excited state lifetime, and thermal stability of the title compounds. The absorption and emission spectra of embodiments [2a-2d] are presented in
All embodiments of complexes are weakly emissive in fluid solutions of deaerated 2-MeTHF with quantum yields (4)) less than 0.01 at room temperature, but become strongly luminescent at 77 K and when doped in PMMA films (
At 298 K, the excited state lifetimes (τ) of embodiments [2a-2d] in fluid solution display multiexponential decays with nano- and microsecond components. The dynamic behavior suggests a possible equilibration between other triplet states before deactivation and is currently under further investigation. Upon cooling 2-MeTHF solutions of embodiments [2a-2d] to 77 K, becomes first-order and ranges from 5.11 μs [2c] to 6.38 μs [2d]. Low temperature emission spectra for embodiments [2a-2d] all display well-defined vibronic features consistent with emission from a ligand-centered triplet state. Introduction of the CH3 group to the nido-carboranyl-pyridyl ligand has a negligible effect on the luminescence, as the E0-0 energies and vibronic structure for embodiments [2a/2b] and [2c/2d] are nearly indistinguishable (
Methylation of the nido-carboranyl fragment has little effect on photophysical properties when these complexes are doped in PMMA films since ϕ, τ, and the emission frequencies for embodiments [2a/2b] and [2c/2d] are roughly identical. Conveniently, the carboranyl moiety can be functionalized to address solubility issues, such as in the case of embodiments [2d to 2c], without significant effect on the emission properties. This is a significant advantage of the carborane-based framework in the context of embodiments of the system.
From the excited-state lifetimes and quantum yields of embodiments [2a-2d] doped in the PMMA matrices, the radiative (kr) and nonradiative (knr) rate constants can be deduced (
Cyclic voltammetry (CV) plots of [2a-2c] are presented in
A series of zwitterionic Ir(III)-based phosphors have been previously probed electrochemically and were shown to display shifts to more positive potentials (1.09 V-1.58 V vs Fc+/Fc) compared to typical Ir(III)-based phosphors containing a formally neutral Ir(III) center (˜0.9 V vs Fc+/Fc). Cyclic voltammetry measurements of an independently synthesized deboronated analogue [4a] of embodiment [1b] were performed, which show the first oxidation wave centered at 0.57 V vs Fc+/Fc. It is therefore suggested that the first oxidation is centered on the nido-carboranyl fragment (whose oxidation is pushed to more positive potentials upon association to the metal center), and the second oxidation corresponds to a metal-centered Ir(III)/(IV) couple. Despite the apparent electrostatic interaction between the carboranyl ligand and the Ir(III) center, embodiments [2a-2d] have proven to be very thermally stable. Thermogravimetric analysis (TGA) shows the onset of mass loss occurring from 320-355° C. for these compounds (
The electronic structures of embodiments [2a-2d] calculated using density functional theory (DFT) provide further insights into the observed photophysical phenomena. Ground-state geometries of embodiments [2a-2d] were optimized from the coordinates obtained from their crystallographically derived X-ray data, and subsequent single-point calculations were carried out with the B3LYP functional and TZP basis set (
Infrared (IR) spectroscopy suggests only weak coordination of the bridging hydride to the metal center: solid-state IR spectra reveal broad resonances in the expected B—H region ˜2500 cm−1, which correspond to the cage B—H stretches, with some fine structure observed. An additional but very weak resonance is observed for embodiments [2a-2d], ˜2100 cm−1, which is suggestive of a weak Ir-μ-H—B stretching band. Such M-μ-H—B interactions have been noted previously with carboranes. In particular, Reed and Teixidor observed similar stretching frequencies in [CB11H12]— (2380 cm−1) and nido-carborane-based (2119-2077 cm−1) systems, respectively, and have also ascribed these bands to weak interactions of carboranyl B—H bonds with cationic metal centers. (See, e.g., Shelly, K., et al., J. Am. Chem. Soc. 1985, 107, 5955; Shelly, K. & Reed, C. A. J. Am. Chem. Soc. 1986, 108, 3117; and Teixidor, F., et al., J. Am. Chem. Soc. 2000, 122, 1963, the disclosures of which are incorporated herein by reference. Hawthorne observed slightly lower B—H stretching frequencies (1965 cm−1) for a nido-carborane anion associated with Ir(III) through two B-μ-H—Ir interactions. (See, e.g., Doi, J. A., et al., J. Chem. Soc., Chem. Commun. 1980, 80, the disclosure of which is incorporated herein by reference.)
Given the rigid steric profile of the ppy ligands around the octahedral iridium center and the bulk of the carboranyl ligand, it is suggested that the bridging hydride interacts with the metal to complete its preferred octahedral geometry but that the primary mode of association results from ion pairing between the formally anionic nido-carborane and the formally cationic Ir(III) center (
Using DFT, it was possible to further probe the interaction between Ir(III) and the nido-carboranyl fragment in embodiments [2a-2d] using the Quantum Theory of Atoms in Molecules (QTAIM) analysis, which has been used to evaluate different types of bonding (e.g., covalent, electrostatic) interactions between atoms. (See, e.g., Bader, R. F. W. Chem. Rev. 1991, 91, 893; and For QTAIM analysis of boron-containing clusters, carboranes, and electron deficient cluster species, see: Bader, R. F. W. & Legare, D. A. Can. J. Chem. 1992, 70, 657; and Bader, R. F. W. Atoms in Molecules: A Quantum Theory; Oxford University Press: New York, 1990, the disclosures of which are incorporated herein by reference.) The results suggest that minimal covalency exists between Ir(III) and either H(1A) or B(11) in embodiment [2a] (
Second, while a BCP is found in embodiments [2a-2d] between Ir and H(1A), the value of the electron density (ρβ) at this point is ˜0.08 for all compounds. In general, ρβ values of 0.2 or greater are indicative of covalent interactions, whereas values of less than 0.1 signify noncovalent interactions such as van der Waals, hydrogen bonding, or electrostatic interactions. The Laplacian of the electron density at the BCP (∇2ρβ) signifies the relative concentration or depletion of electron density along and perpendicular to the bond path at the BCP. Positive values generally indicate the depletion of electron density at the BCP, which is indicative of closed-shell bonding interactions, such as ionic and hydrogen bonding. Values of ˜0.22 are obtained for all structures, strongly suggesting closed shell/electrostatic interactions between the carboranyl ligand fragment and Ir(III).
Accordingly, embodiments are directed to electrostatically bound ligands for Ir(III)-based phosphors. Various embodiments use bulky, weakly coordinating, noncovalent ligand frameworks for stable and emissive phosphorescent molecules based on Ir(III). Importantly, embodiments allow for the structural modification of the weakly coordinating ligand to be carried out without detrimentally affecting the photophysical properties of the resulting complex: the inclusion of a methyl group at the Cvertex of the nido-carboranyl ligand in embodiments [2a] and [2c] does not strongly influence the emission wavelength relative to the nonmethylated counterparts (embodiments [2b] and [2d], respectively); importantly, however, methylation does improve the solubility of embodiments [2a and 2c] relative to [2b and 2d]. Embodiments utilize this orthogonality as a potentially useful handle for optimizing the physical/materials properties of this class of Ir(III)-based phosphors without significantly modulating the excited-state characteristics when employed as a component of an OLED construct, particularly given the nontriviality of engineering dopant-host layer compatibility. (See, e.g., Swensen, J. S., et al., Adv. Funct. Mater. 2011, 21, 3250; Tsang, D. P.-K., et al., Org. Electron. 2011, 12, 1114; and Veinot, J. G. C. & Marks, T. J. Acc. Chem. Res. 2005, 38, 632, the disclosure of which is incorporated herein by reference.)
Embodiments may also be coupled with methods described elsewhere herein to functionalize boron vertices of carboranes with vertex precision to provide powerful strategies for modulating structural and photophysical properties of Ir(III) species with B-substituted carborane-based ligands. The utility of such boron cluster-based weakly coordinating ligands in phosphorescent molecules demonstrated in accordance with embodiments also enabled the use of other tunable boron cluster congeners that similarly present appreciable steric bulk and overall negative charge. (See, e.g., Lavallo, V., et al., Angew. Chem., Int. Ed. 2013, 52, 3172; Kultyshev, R. G., et al., J. Am. Chem. Soc. 2002, 124, 2614; Beletskaya, I. P., et al., J. Organomet. Chem. 2004, 689, 2920; Kultyshev, R. G., et al., Inorg. Chem. 2003, 42, 3199; Himmelspach, A., et al., Inorg. Chem. 2012, 51, 2679; Douvris, C. & Michl, J. Chem. Rev. 2013, 113, PR179; Preetz, W. & Peters, G. Eur. J. Inorg. Chem. 1999, 1999, 1831; Semioshkin, A., et al., Polyhedron 2004, 23, 2135; Olid, D., et al., Chem. Soc. Rev. 2013, 42, 3318; Peymann, T., et al., Inorg. Chem. 2000, 39, 1163; Grüner, B., et al., J. Am. Chem. Soc. 1999, 121, 3122; Zhang, Y., et al., S. Eur. J. Inorg. Chem. 2015, 2015, 5158; Konieczka, S. Z., et al., Eur. J. Inorg. Chem. 2013, 2013, 134; Bolli, C., et al., Chem.-Eur. J. 2014, 20, 13783; Wong, Y. O., et al., Chem.-Eur. J. 2016, 22, 6764; Ivanov, S. V., et al., J. Fluorine Chem. 1998, 89, 65; Ivanov, S. V., et al., Inorg. Chem. 2003, 42, 4489; Boron Hydride Chemistry Muetterties, E. L., Ed., Academic Press, Inc: New York, N.Y., 1975; Ramirez-Contreras, R., et al., Angew. Chem., Mt. Ed. 2013, 52, 10313; Press, L. P., et al., Chem. Commun. 2015, 51, 14034; and Ramirez-Contreras, R. & Ozerov, O. V. Dalton Trans. 2012, 41, 7842, the disclosures of which are incorporated herein by reference.) In various embodiments, functionalized closo-boron clusters, such as the anionic carba-closo-dodecaboranes and charge-compensated closo-dodecaborates, may be incorporated into embodiments, as these bulky, closo-clusters are generally more stable than nido- or arachno-derivatives and are themselves widely used as noncoordinating anions. In short, embodiments provide methods for strategically designing, weakly coordinating carborane-based ligands based on the materials and photophysical properties of metal-based luminescent molecules to produce efficient emitters for application in light-emitting devices.
Formation of Atomically Precise Cluster Nanomolecules
Embodiments are also directed to methods for forming atomically precise and highly tunable hybrid nanomolecules with well-defined three-dimensionality. In various embodiments perfunctionalization of atomically precise clusters with pentafluoroaryl-terminated linkers produces size-tunable rigid cluster nanomolecules amenable to facile modification with a variety of thiol-containing molecules and macromolecules. In some embodiments, assembly proceeds at room temperature within hours under mild conditions, and the resulting nanomolecules exhibit high stabilities because of their full covalency. Various embodiments also demonstrate how these nanomolecules may be grafted with saccharides to exhibit dramatically improved binding affinity towards a protein. Ultimately, the embodiments allow for the rapid generation of precise molecular assemblies to investigate multivalent interactions.
Natural systems feature very complex three-dimensional (3D) molecular architectures that can interact with a high degree of specificity and fidelity. Among the well-established interaction modes, multivalency has been known to enable myriad biological events by strengthening individually weak interactions between biomolecules that are either native or foreign to the organism. (See, e.g., Mammen, M., Choi, S.-K. & Whitesides, Angew. Chem. Int. Ed. 37, 2754-2794 (1998), the disclosure of which is incorporated herein by reference.) Multivalent interactions can be found in such diverse processes as infection (viral/bacterial proteins-cell receptors), immune recognition (antibodies-cell receptors/antigens, cytokines-cell receptors) and gene-expression regulation (transcription factors-DNA) because of the higher avidity and better recognition compared with the corresponding monovalent bindings. (See, e.g., Kiessling, L. L., Gestwicki, J. E. & Strong, L. E. Angew. Chem. Int. Ed. 45, 2348-2368 (2006), the disclosure of which is incorporated herein by reference.)
Inspired by nature's design, chemists have taken an interest in developing synthetic multivalent ligands with the ability to bind specific target receptors with a high affinity to (1) elucidate the mechanistic details of multivalent interactions and (2) promote or inhibit biological interactions of interest. (See, e.g., Jones, L. H., Nat. Chem. 7, 952-960 (2015), the disclosure of which is incorporated herein by reference.) Many examples of synthetic scaffolds have emerged over the past several decades, which include, but are not limited to, polymeric nanoparticles, dendrimers, and hybrid nanoparticles. (See, e.g., Elsabahy, M. & Wooley, K. L., Chem. Soc. Rev. 41, 2545-2561 (2012); Rao, J. P. & Geckeler, K. E., Prog. Polym. Sci. 36, 887-913 (2011); Tomalia, D. A. et al., Polym. J. 17, 117-132 (1985); Hawker, C. J. & Frechet, J. M., J. Am. Chem. Soc. 112, 7638-7647 (1990); Farokhzad, O. C. & Langer, R. ACS Nano 3, 16-20 (2009); Peer, D. et al., Nat. Nanotech. 2, 751-760 (2007); Daniel, M.-C. & Astruc, D., Chem. Rev. 104, 293-346 (2004); Dreaden, E. C., et al., Chem. Soc. Rev. 41, 2740-2779 (2012); Brust, M., et al., J. Chem. Soc., Chem. Commun. 801-802 (1994); Giljohann, D. A. et al., Nano Lett. 7, 3818-3821 (2007); Jones, M. R., et al., Science 347, 1260901 (2015); Suzuki, K., Sato, S. & Fujita, Nat. Chem. 2, 25-29 (2010); Heindl, C., et al., Am. Chem. Soc. 137, 10938-10941 (2015); Ambrogio, M. W., et al., Acc. Chem. Res. 44, 903-913 (2011), the disclosures of which are incorporated herein by reference.) Specifically, the advent of nanotechnology and the development of surface-functionalized metal nanoparticles has provided an extremely powerful class of multivalent scaffolds. For example, gold nanoparticles (AuNPs) capped with thiolated ligands can feature biocompatibility and stability, which enables them for applications that require binding and recognition capabilities. Hybrid AuNP systems are especially attractive because of the synthetic ease of producing systems that are well-defined and tunable in size. Nevertheless, it is well known that thiolated ligands often can desorb or undergo exchange processes with other surfactants in solution over short periods of time, and furthermore, various electrochemical conditions or elevated temperatures (>60° C.) dramatically accelerate these processes. (See, e.g., Love, J. C., et al., Chem. Rev. 105, 1103-1170 (2005); Hostetler, M. J., et al., J. Am. Chem. Soc. 118, 4212-4213 (1996); Hostetler, M. J., Templeton, A. C. & Murray, R. W., Langmuir 15, 3782-3789 (1999); and MacLeod, M. J. & Johnson, J. A., J. Am. Chem. Soc. 137, 7974-7977 (2015), the disclosures of which are incorporated herein by reference.) These events can be explained primarily by the relatively weak nature of the gold-thiolate bond (40-50 kcal mol−1). Processes of thiol-ligand exchange also readily occur on smaller Au-based cluster molecules (≤5 nm), which potentially limits the ability of researchers to create atomically precise hybrid nanomolecules that remain compositionally well-defined under biologically relevant conditions (for example, in serum). (See, e.g., Hakkinen, H., Nat. Chem. 4, 443-455 (2012), the disclosure of which is incorporated herein by reference.)
Embodiments provide a strategy to build robust atomically precise hybrid nanomolecules using air-stable inorganic clusters densely decorated with perfluoroaromatic functional groups. (See, e.g, Yvon, C. et al., Angew. Chem. Int. Ed. 53, 3336-3341 (2014); Gouzerh, P. & Proust, A., Chem. Rev. 98, 77-112 (1998); Müller, A. & Gouzerh, P., Chem. Soc. Rev. 41, 7431-7463 (2012); Li, G., et al., J Inorg. Organomet. Polym. 11, 123-154 (2001); Spokoyny, A. M., Pure Appl. Chem. 85, 903-919 (2013); and Lee, I. S., et al., J. Am. Chem. Soc. 127, 13802-13803 (2005), the disclosures of which are incorporated herein by reference.) Using this organomimetic strategy according to embodiments, it is possible to mimic the rigid surface of a Au-based nanoparticle core and simultaneously produce assemblies that are fully covalent and thus stable under relatively harsh conditions (
Given the high reactivity of the perfluoroarenes with thiol-based nucleophiles, embodiments utilize perfluoroaryl-thiol SNAr chemistry to conjugate various thiolated groups onto perfluoroaryl-containing clusters efficiently under mild conditions at room temperature. (See, e.g., Birchall, J. M., et al., Chem. Commun. Lond. 338-339 (1967); Becer, C. R., et al., Angew. Chem. Int. Ed. 48, 4900-4908 (2009); Becer, C. R. et al., Macromolecules 42, 2387-2394 (2009); and Spokoyny, A. M. et al., J. Am. Chem. Soc. 135, 5946-5949 (2013), the disclosures of which are incorporated herein by reference.) Embodiments may also be combined with the rapid perfunctionalization embodiments of the [B12(OH)12]2− cluster previously described. As described, such methods and embodiments feature a wide scope of substituents and allow for the synthesis of perfunctionalized clusters grafted with rigid linkers that contained peripheral pentafluoroaryl moieties (
Conjugation studies were conducted between [2] and 1-hexanethiol [A] to show that [2] and [3] can be fully functionalized by thiols via an SNAr reaction, in accordance with embodiments. Cluster [2] was mixed with 12 equiv. of thiol [A] in dimethylformamide (DMF) in the presence of base and left stirring under a N2 atmosphere to mitigate the undesired oxidation of the thiol reagent. Notably, the initially dark-red solution quickly turned colorless. 11B NMR spectroscopy of this colorless solution revealed a singlet resonance at δ=15, characteristic of a reduced cluster in a [2]2− oxidation state, which is consistent with the reducing capacity of the thiolate species when exposed to [2]0 (
19F NMR spectroscopy was utilized to monitor the conversion of [2] into [2a], given the diagnostic change associated with this transformation (
Overall, these results suggest that, with embodiments of the method, it is possible to assemble OCNs rapidly via SNAr chemistry under very mild and operationally simple conditions that mimic the simplicity of the assembly of thiol-capped AuNPs. Furthermore, unlike the previously developed Huisgen ‘click’ cycloaddition and carbamate functionalization strategies of inherently non-rigid B12-based clusters, which require elevated temperatures, long reaction times (days) and a large excess of reagents (4-5-fold per vertex), the perfluoroaryl-thiol SNAr chemistry described here in accordance with embodiment proceeds using significantly milder conditions. (See, e.g., Jalisatgi, S. S. et al., J. Am. Chem. Soc. 133, 12382-12385 (2011), the disclosure of which is incorporated by reference.)
Thiol-capped AuNP constructs are also extremely attractive given the chemical orthogonality of the gold-thiol interaction compared with that of other ligands, which provides an opportunity to use a wide variety of unprotected thiol reagents for facile and programmable self-assembly. Therefore, embodiments also utilize an SNAr chemistry on perfluorinated clusters to mimic this attractive feature. To evaluate the thiol selectivity of embodiments of the approach, conjugation reactions between [2] and thiols are performed that featured additional nucleophilic groups, such as alcohols and amines. Consistent with the previous work by Pentelute and co-workers with unprotected peptides, it is found that the model thiol species [D-F] all reacted with [2] through the thiol site selectively to form the desired perfunctionalized OCNs [2d-2f] (
With the successful perfunctionalization of [2] (vide supra), embodiments may be extended into larger-sized clusters [3] that could be perfunctionalized with the same thiols to create a new generation of OCNs that are modularly extended in size, but could also accommodate 12-fold conjugation with bulkier substrates. Indeed, under the same conditions as described above for the functionalization of [2], cluster [3], in accordance with embodiments, undergoes clean and facile perfunctionalization chemistry with thiols [A-F] to yield embodiments [3a-3f] (
To demonstrate that embodiments could introduce more-complex molecular architectures onto the clusters, poly(ethylene glycol) (PEG) may be used. (See, e.g., Hoffman, A. S., J. Control. Release 132, 153-163 (2008); and Alconcel, S. N. S., Baas, A. S. & Maynard, H. D., Polym. Chem. 2, 1442-1448 (2011), the disclosures of which are incorporated herein by reference.) Complete 12-fold conjugation between [2] and commercially available mPEG-thiol (Mw=356 Da) occurred within 24 hours at room temperature to yield OCN [2i] (
The stability of the conjugation linkage between the cluster core and the thiol was then examined. Given the full covalency of [2i], it might be expected that it should not undergo ligand-exchange, a process that commonly occurs with many ligand-capped AuNPs. Significantly, no thiol-exchange occurred when [2i] (0.8 mM) was exposed to 2-mercaptoethanol (20 mM) over a period of 11 days. Similar results were obtained with 2 mM glutathione. Overall, these results clearly demonstrate that the OCNs constructed via the SNAr approach in accordance with embodiments feature superior robustness compared with many AuNP-based assemblies.
PEGylated OCNs in accordance with embodiments were characterized by a number of techniques to ensure their proposed nearly monodisperse composition (whereas the OCN cores are monodisperse, the PEG chains used feature some compositional variability because of the inherent limitations of PEG oligomer synthesis). (See, e.g., Veronese, F. M. & Pasut, G., Drug Discov. Today 10, 1451-1458 (2005), the disclosure of which is incorporated herein by reference.) First, 2D diffusion ordered spectroscopy (2D DOSY)1H NMR were conducted with purified samples of [2i-2k] and the more-extended OCNs [3i-3k] (
To determine the size of a single non-aggregated OCN [3i], additional transmission electron microscopy (TEM) experiments were performed on [3i] (
After demonstrating the scope of embodiments with various classes of thiols, the scaffold clusters may be coated with recognition moieties to develop OCNs capable of multivalent binding interactions. In nature, multivalent glycoconjugates, such as glycoproteins and glycolipids, can bind lectins with a relatively high avidity, and thereby bypass the fundamental limitation of weak monosaccharide binding (dissociation constants (KD) range between millimolar and micromolar). (See, e.g., Dam, T. K., et al., J. Biol. Chem. 275, 14223-14230 (2000) & Bernardi, A. et al., Chem. Soc. Rev. 42, 4709-4727 (2013), the disclosures of which are incorporated herein by reference.) In such embodiments, clusters [2] and [3] can serve as rigid, tunable scaffolds for the 3D precise display of saccharides. In some such embodiments, using commercially available glucose precursor 1-thio-3-D-glucose tetraacetate, it is possible to synthesize the functionalized OCNs [2l] and [31] featuring [12] appended glucose molecules (
Surface plasmon resonance (SPR) experiments were then conducted with a Biacore T100 instrument to monitor and quantify binding interactions between the glycosylated OCN [2l] and a model lectin concanavalin A (ConA) at pH 7.4. ConA was covalently attached to the Au-coated sensor chip's dextran layer via conventional amide coupling, and binding between ConA and the injected analyte was measured as a change in the refractive index (RI) and expressed in response units (RU). From the binding sensorgrams (
Although not to be bound by theory, the glycosylated OCN's dramatically enhanced affinity over D-glucose towards ConA can be explained by the cluster glycoside effect. To better understand the mechanistic details of the binding between [2l] and ConA, MD simulations of the interactions between [2l] and ConA were performed (see the snapshots of the simulation in
Accordingly, embodiments have been developed that allow a rapid assembly of fully covalent nanoparticles with atomic precision. Specifically, embodiments demonstrate that the rigid clusters densely decorated with perfluoroaryl-containing functional groups undergo efficient conjugation with a variety of thiols via SNAr chemistry under very mild conditions at room temperature. Embodiments of this chemistry are reminiscent of the chemoselective assembly conditions associated with thiol-capped AuNPs, and similarly to thiol-capped AuNPs, these OCNs can be easily tuned in size and surface chemistry by choosing a specific thiol reagent. OCNs according to embodiments exhibit dramatically improved structural stability under a wide range of biologically relevant conditions because of the full covalency of all the bonding interactions that comprise these nanomolecules. Using embodiments of this assembly strategy it is possible to design and synthesize nanomolecules that feature a 3D densely packed layer of saccharides that can participate in multivalent binding with a natural lectin and lead to a dramatic increase in binding affinity. Embodiments open a methods to create highly tailored synthetic mimics of ligand-capped AuNPs that feature rigid and fully covalent atomically precise assemblies.
Engendering Abiotic Protein-Like Functions in Cluster-Based Atomically Precise Scaffolds.
In embodiments, these constructs may be used as antibody mimics to bind proteins. Embodiments develop multivalent species capable of binding and sensing complex biomolecules. In contrast to existing hybrid nanoparticles, the system features improved stability towards harsh environmental conditions including pH, oxidants/reductants and serum.
In order to ascertain whether the formed structures possess improved stability stemming from their complete covalency and proximal packing of the functional groups, a series of systematic stability studies may be performed on the system. Results indicate that embodiments of the thiol-functionalization chemistry are amenable towards complex unprotected peptides (
To assess in vitro protease resistance of the antibody mimics, it is possible to use various proteases such as trypsin, chymotrypsin, and proteinase K based on the sequence composition of the biomolecule. Time-dependent cleavage of amide bonds will be monitored by LCMS to determine rates of degradation, and will be compared to that of the AuNPs and free peptide.
To determine proteolytic stability in serum: constructs may be incubated with fresh serum at 37° C. for various time points. The serum samples may then be flash frozen, lyophilized, extracted with acetonitrile/water solution containing TFA, and subjected to targeted LCMS/MS for quantification of intact peptides. If the previous approach fails, biotin may be installed on each variant and use for sample cleanup and enrichment with streptavidin beads after incubation with serum. Then LCMS can be used to obtain the proteolytic profile and degradation rates to determine if the scaffold significantly stabilizes the variants in ex vivo serum. The effect of spacer linkers on the structure and the function of these biomolecules may be determined using CD spectroscopy, X-ray crystallography, NMR spectroscopy, and molecular dynamics simulations (for peptides). Specifically, CD spectroscopy may be used to monitor the effects of linker length and architecture on secondary structure of grafted peptides, e.g. the extent of a-helical conformation by examining the dual minima at 208 and 222 nm in CD spectra. Embodiments show the formation of a-helical motif on model peptide is enhanced, although not to be bound by theory, likely as a function of packing. High resolution NMR spectroscopic may be used to gain more insight into the 3D structures of these assemblies according to embodiments. For example, TOCSY NMR measurements may be used to ascertain and correlate the ordering observed via the structures via CD spectroscopy. NOESY and ROESY NMR experiments under various pH conditions may be used to obtain a precise 3D structure of these assemblies. Finally, X-ray crystallography may be used to further elucidate precise three-dimensional structures and understand the role of the size and dynamics in embodiments of the system.
Utilizing Atomically-Precise Multivalency for Biomolecular Recognition and Sensing.
Many embodiments are directed to protein mimics, where one inorganic scaffold can now tether multiple receptor molecules with a three-dimensional precision. These species can be conceptually thought of as abiotic antibody mimics in the way they can selectively associate with complex targets. Specifically, many embodiments are directed analogous peptide-based abiotic assemblies that can interact with DNA thereby mimicking certain functions of histones.
Virus Capsid Recognition and Sensing.
In many embodiments assemblies are configured to recognize and sense two structurally and functionally distinct systems. In one embodiment a gp41 viral scaffold (
Previously, researchers developed several classes of peptide molecules capable of binding gp41, however these binding affinities remain relatively small. Importantly, as opposed to polydisperse nanoparticles and polymers, atomically precise scaffolds in accordance with embodiments will be fully amenable to structural studies via classical protein characterization methods such as X-ray crystallography and Nuclear Magnetic Resonance spectroscopy allowing to precisely pinpoint interactions between these species and a protein target. Peptide sequences may be used that are designed to bind a single helix of gp41 (
Atomically Precise Cationic Nanomolecules as Histone Mimics.
Ability of polycationic agents to interact with the negatively charged phosphate backbone of the oligonucleotides has been recognized for a long time. (See, e.g., Su, C.-J., et al., Macromolecules 2012, 45, 5208-5217; and Yu, S. and Larson, R. G., Soft Matter 2014, 10, 5325-5336, the disclosures of which are incorporated herein by reference.) This observation has led to the development of many intracellular delivery platforms and detection assays. In fact, nature has been utilizing such a class of interactions DNA packaging via condensation. This process is centered around histone protein assemblies which consist of several subunits with a precisely regulated positive charge density located in a three-dimensional space occupying approximately 11 nm diameter (
2D and 3D Materials Featuring Atomically Precise Clusters Nanomolecules.
Embodiments are also directed to a reliable technique where 3D-based multivalency can be precisely measured and quantified in a more high-throughput fashion would carry a tremendous advantage. In some embodiments a new class of conductive 2D materials, which can be integrated into the existing surface-plasmon resonance technology (SPR) thereby allowing to precisely measure molecular binding events (
Recent interest in two-dimensional (2D) materials, such as graphene, has spurred a significant research effort in creating design rules allowing deliberate synthesis of new classes of such materials. 2D materials show potential promise in electronics, sensors, and catalysts. (See, e.g., Geim, A. K., Novoselov, K. S., Nature Materials 2007, Volume 6, 183-191; and Allen, M. J., et al., Chem. Rev. 2010, 11, 132-145, the disclosures of which are incorporated herein by reference.) For example, graphene, a 2D honeycomb-like network of carbon, is an excellent candidate material for electronics due to its extremely high conductivity. Graphene's high conductivity stems from a continuous 2D π-orbital conjugation, which allows electrons to freely flow along the graphene surface. However, π-orbitals of one layer can overlap with it-orbitals of another layer resulting in π-π stacking interactions that hold two or more sheets of this material together. In some cases, the unique property of the 2D material diminishes, as additional layers are stacked together. This prompted researchers to look for general methods to exfoliate individual sheets of graphene and similar 2D materials. Although 2D conjugated molecules have been extensively studied and used to create 2D materials, there are no reports addressing the possibility for utilizing three-dimensional (3D) aromatic molecules to create 2D monolayer-structured materials. In order to synthesize an “ideal” 2D material consisting of aromatic boron clusters one needs to address the following two challenges: 1) identify whether the incorporation of boron clusters in 2D sheets can suppress π-π interactions leading to self-exfoliated materials 2) develop the design rules allowing one to maximize electronic conductivity in the polymers consisting of 3D aromatic boron clusters and 3) develop post-synthetic modification tools on the corresponding materials allowing to selectively graft ligand moieties around the cluster species.
Accordingly, embodiments are directed to a class of carborane-containing covalent organic frameworks. Covalent organic frameworks (COFs) are crystalline organic supramolecular arrays composed of molecular building blocks. (See, e.g., El-Kaderi, H. M., et al., Science 2007, Volume 316, 268-272; Farha, O. K., et al., Chemistry of Materials 2009, Volume 21, 3033-3035; Kuhn, P., et al., Angew. Chem., Int. Ed. 2008, Volume 47, 3450-3453; DeBlase, C. R., et al., Chem. Mater. 2015, 9, 3178-3183; Smith, B. J., et al., J. Am. Chem. Soc. 2014, 136, 8783-8789; and Duhovic, S. and Dinc{hacek over (a)}, M., Chem. Mater. 2015, 27, 5487-5490, the disclosures of which are incorporated herein by reference.) COFs were previously constructed from it-conjugated molecules and shown to exhibit a high degree of π-conjugation. Consequently, COF sheets exhibit pronounced π-π stacking interactions. Functionalizing the molecular building blocks with carborane derivatives presents an opportunity to develop COF systems with suppressed π-π interactions, since boron clusters lack cofacially exposed it aromatic orbitals (
In order to achieve highly functionalized boron clusters it is important to identify regio- and chemospecific transformations on the boron clusters that can serve as building blocks to construct 2D materials. Previously, it has been shown that by virtue of incorporating multiple cyanide groups within organic molecules, one could assemble conducting COF materials. In order to achieve this goal, a new cross-coupling chemistry that allows one to precisely graft cyanide functional groups on the boron vertices of carborane cluster has been developed. For example, 9-bromo-metacarborane species can be converted into the corresponding cyano derivative in 90% yield (
Alternative Cluster Constructs
Some embodiments are directed to the synthesis of fully alkylated closo-hexaborate dianions. In various embodiments, the reaction of [NBu4][B6H6Hfac], benzyl bromide, and triethylamine under microwave heating conditions affords persubstituted [NBu4][B6(CH2AR)6Hfac] (Ar=C6H5, 4-Br—C6H4), which have been isolated and characterized by NMR spectroscopy, mass spectrometry, single crystal X-ray diffraction, and other spectroscopic techniques. Electrochemical studies of embodiments of these clusters reveal an irreversible one-electron oxidation likely indicating degradative cage rupture. The observed metal-free alkylation in accordance with embodiments proceeds as a consequence of the pronounced nucleophilic character of the hexaborate anion. Embodiments represent the first example of a perfunctionalized hexaborate cluster featuring B—C bonds.
Many polyhedral boron clusters have been shown to exhibit enhanced stability relative to more commonly encountered tricoordinate boranes. This stability has been ascribed to the unique bonding arrangement and three-dimensional aromatic character of these polyhedral clusters. (See, e.g., King, R. B.; Rouvray, D. H. J. Am. Chem. Soc. 1977, 99, 7834; Aihara, J.-I. J. Am. Chem. Soc. 1978, 100, 3339; Bridgeman, A. J. & Empson, C. J. Chem. Sci. 2008, 32, 1359; Housecroft, C. E., et al., Polyhedron 1985, 4, 1875; Zhao, M. & Gimarc, B. M., Inorg. Chem. 1993, 32, 4700; and King, R. B. Chem. Rev. 2001, 101, 1119, the disclosures of which are incorporated herein by reference.) For example, the B12H122− dianion is one of the most kinetically stable compounds known, capable of withstanding strongly acidic, oxidizing, and basic conditions, as well as heating in air beyond 600° C. (See, e.g., Pitochelli, A. R. & Hawthorne, M. F. J. Am. Chem. Soc. 1960, 82, 3228-3229; and Muetterties, E. L., et al., Inorg. Chem. 1964, 3, 444-451, the disclosures of which are incorporated herein by reference.) Partial and exhaustive functionalization of this cluster can furnish unique molecular scaffolds, which are potentially useful for a wide range of applications including, but not limited to, photoactive materials, polymers, electrolytes, catalysts, therapeutics, and diagnostic agents in biomedicine.
(See, e.g., Grimes, R. N. J. Chem. Ed. 2004, 81, 657; Kaim, W. et al., Angew. Chem. Int. Ed. 2009, 48, 5082; Nunez, R, et al., F. Chem. Rev. 2016, 116, 14307; Peymann, T., et al., Inorg. Chem. 2001, 40, 1291; Peymann, T., et al., J. Am. Chem. Soc. 1999, 121, 5601; Peymann, T. et al., Chem. Commun. 1999, 2039; Ivanov, S. V. et al., J. Am. Chem. Soc. 2003, 125, 4694; Peryshkov, D. V. et al., J. Am. Chem. Soc. 2010, 132, 13902; Nieuwenhuyzen, M et al., Inorg. Chem. 2009, 48, 889; Boeré, R. T. et al., Chem. Eur. J. 2014, 20, 4447; Maderna, A. et al., Angew. Chem. Int. Ed. 2001, 40, 1661; Zhang, Y. et al., Eur. J. Inorg. Chem. 2015, 5158; Gu, W. et al., Inorg. Chem. 2011, 50, 2726; Van, N. et al., Chem. Eur. J. 2010, 16, 11242; Messina, M. S. et al., J. Am. Chem. Soc. 2016, 138, 6952; Ma, L. et al., Inorg. Chem. 2006, 45, 278; Lee, Jr., M. W. Angew. Chem. Int. Ed. 2017, 56, 138; Hawthorne, M. F. Angew. Chem. Int. Ed. 1993, 32 950; Kultyshev, R. G. et al., J. Am. Chem. Soc. 2002, 124, 2614; Satapathy, R. et al., J. Organomet. Chem. 2015, 798, 13; Sivaev, I. B., et al. Russ. Chem. Bull. Int. Ed. 2002, 51, 1362; Nakamura, H. et al., Org. Biomol. Chem. 2012, 10, 1374, the disclosures of which are incorporated herein by reference.) The ability to design and tune these molecules remains crucial for producing desirable properties and reactivity.
In general, two main approaches to persubstituted Group 13 polyhedral clusters in accordance with embodiments exist. The first involves the assembly of prefunctionalized fragments to form the desired cluster-based motif (
Beyond icosahedra, other polyhedral boron clusters are known, and in contrast to the well-established chemistry of the B12H122− dianion and its derivatives, the chemistry of the closo-hexaborate dianion, B6H62−— the smallest of the known deltahedral 3D aromatic boron clusters—has received much less attention. Predicted in 1954 and isolated in 1964, the B6H62− dianion, which is stable under ambient conditions both in the solid and solution state, was quickly shown to be rather different than its icosahedral relative. (See, e.g., Eberhardt, W. H. et al., J. Chem. Phys. 1954, 22, 989; Longuet-Higgins, H. C. & de V. Roberts, M. Proc. Royal Soc. London, A 1954, A224, 336; Longuet-Higgins, H. C. & de V. Roberts, M. Proceedings of the Royal Society of London A, 1955, A230, 110; and Boone, J. L. J. Am. Chem. Soc. 1964, 86, 5036, the disclosures of which are incorporated herein by reference.) The pioneering work of Preetz revealed the apparent nucleophilic character of the hexaborate clusters to be significantly more pronounced than the B12H122− species. (See, e.g., Preetz, W.; Peters, G. Eur. J. Inorg. Chem. 1999, 1831, the disclosure of which is incorporated herein by reference.) This observation led to some early examples demonstrating that B6H62− can undergo partial substitution with carbon-based electrophiles to form B—C bonds; similar reactions with the dodecaborate scaffold have not been disclosed. To date, persubstitution of the hexaborate cluster has never been accomplished. Here embodiments provide the synthesis and properties of the first peralkylated hexaborate clusters, B6(CH2Ar)62− (Ar=C6H5, 4-Br—C6H5), generated as a consequence of the nucleophilic character of the hexaborate dianion.
Preetz and co-workers previously disclosed several examples of alkylated hexaborate clusters of the type B6RnH6-n2− (n=1-3, R=alkyl) and it was ultimately suggested that alkylation would not proceed beyond three substitutions. B—C bond formation is thought to occur with concomitant migration of the terminal H from the B vertex to an adjacent face of the hexaborate cluster. This facial proton (Hfac) mitigates the nucleophilicity of the cluster and must be removed with base for further substitutions to occur. In the examples reported by Preetz, it was concluded that that removal of Hfac was not possible beyond three B—C bond formations. (See, Preetz, cited above.) Using embodiments of microwave-assisted functionalization analogous with those described above with respect to B12H122− with alkyl electrophiles, it is found possible to produce fully functionalized B6H62− frameworks, bypassing previously encountered limitations.
In accordance with embodiments, treatment of [NBu4][B6H6Hfac] with 30 equivalents of benzyl bromide and Hünig's base in CH3CN under microwave heating conditions led to the formation of a new species displaying a single, broad resonance at δ−7.6 in the 11B NMR spectrum. Further optimization of the reaction conditions permitted the isolation of [NBu4][B6H6Hfac][1a] after work-up in 65% yield (
X-ray diffraction of crystals of [1a] revealed significant disorder due to “wagging” of the benzyl substituents, which was also observed for [B6H5(CH2Ph)]2−. A functionalized benzyl electrophile was therefore employed in an attempt to impart greater order and crystallinity in the desired persubstituted product. Treatment of [NBu4][B6H6Hfac] with 4-bromobenzyl bromide under otherwise identical conditions used to synthesize [1a] similarly affords a compound that displays a single broad peak in the 11B NMR spectrum at δ−7.6 and an IR spectrum consistent with [1a] (
An X-ray diffraction study was carried out on single crystals of [1b] grown from a cooling solution of [1b] in boiling ethanol. [1b] crystallizes in the P21 space group with two independent ion pairs in the asymmetric unit. One NBu4+ counterion is detected per cluster, supporting the proposed facially protonated species and consistent with the 1H NMR data.
While definitive location of the facial proton (Hfac) proved difficult, its position can be tentatively assigned based on the bond metrics of the B6-based core. The B1-B2-B3 face contains the three of the four longest B—B distances in the cluster (1.818, 1.818, and 1.789 Å), which are large in comparison to the average of all other B—B distances, 1.725 Å (range 1.713-1.824 Å). Although not to be bound by theory, it is therefore suggested that Hfac is bound to this face of the cage in the solid state. This assignment is consistent with previous reports. (See, e.g., Baurmeister, J. et al., Naturforsch. 1995, 50b, 623, the disclosure of which is incorporated herein by reference.) All B—C bonds range from 1.592 Å-1.601 Å, which are consistent with the B—C bond distances in previously reported monobenzylated clusters.
While the homo- and heteroleptic perhalogenation (Cl, Br, I) of B6H62− has been reported, embodiments of [1a-b] are the first molecules of their type in which carbon-based substituents are bound to each vertex of the hexaborate cage. (See, e.g., Preetz, W. & Fritze, J. Z. Naturforsch. 1984, 39b, 1472; Fritze, J. et al., Z. Naturforsch. 1987, 42b, 287; Fritze, J. & Preetz, W. Z. Naturforsch. 1987, 42b, 293; Preetz, W. & Stallbaum, M. Z. Naturforsch. 1990, 45b, 1113; Thesing, J.; Stallbaum, M.; Preetz, W. Z. Naturforsch. 1991, 46b, 602, the disclosures of which are incorporated herein by reference.) Indeed, the only other reports of perfunctionalized hexaborate clusters are the charge-neutral B6(NR2)6 species (R=Me, Et). In contrast to embodiments [1a-b], the B6(NR2)6 clusters irreversibly open into cyclic constitutional isomers when heated. Although not to be bound by theory, the formation of embodiments [1a-b] appears to proceed via a simple SN2 mechanism.
Perhalogenated clusters B6X62− (X=Cl, Br, I), mixed halogen clusters B6XnX′6-n2− (X=F, Cl, Br, I; F=1 only), and B6X5R2− (R=alkyl) were previously shown to exhibit redox behavior. (See, e.g., Lorenzen, V., et al., Inorg. Chem. 1998, 37, 4011; Speiser, B.; Wizemann, T.; Wiirde, M. Inorg. Chem. 2003, 42, 4018; and Wanner, M. et al., Z. Naturforsch. 1999, 54b, 1103, the disclosures of which are incorporated herein by reference.) Based on this history, the electrochemical behavior of embodiments, [1a-b] was studied with cyclic voltammetry (CV). Solutions of [1a] and [1b] in anhydrous CH3CN display apparent irreversible one-electron oxidation waves at 0.32 V and 0.46 V vs. Fc/Fc+, respectively (
As the scan rate is incrementally raised from 100 mV/s to 750 mV/s for [1a], a reverse reductive wave becomes more pronounced (
The electronic structure of [1b] was probed using Density Functional Theory (DFT) at the BP86-D3/TZP level of theory and the frontier molecular orbital diagrams obtained from this study are presented in
To investigate the unique bonding structure of [1a] and [1b], X-ray photoelectron spectroscopy (XPS) measurements were performed to further probe the electronic landscape of the B6-based core (
In summary, embodiments are also directed to the perfunctionalization of the hexaborate dianion, which is achievable via treatment with benzyl halides, resulting in the formation of six B—C bonds per cluster. Embodiments also provide for hexaborate clusters that may be (per)functionalized with other electrophiles to form B—R bonds of varying types. Embodiments of the compounds, which are stable solids under ambient conditions, exhibit irreversible electrochemical oxidations, likely the result of cage degradation, ultimately suggesting a differing reactivity from embodiments the peralkylated dodecaborate (B12R122−/1−) species.
DOCTRINE OF EQUIVALENTSAs can be inferred from the above discussion, the above-mentioned concepts can be implemented in a variety of arrangements in accordance with embodiments of the invention. Accordingly, although the present invention has been described in certain specific aspects, many additional modifications and variations would be apparent to those skilled in the art. It is therefore to be understood that the present invention may be practiced otherwise than specifically described. Thus, embodiments of the present invention should be considered in all respects as illustrative and not restrictive.
Claims
1. A metal-free photooxidant comprising an icosahedral dodecaborate consisting of B12(OR)12, where R is a substituent selected from the group consisting of CH2C6F5, CH2(4-CF3C6H4), and CH2(3,5-(CF3)2C6H3).
2. A molecular scaffold for forming atomically precise nanomolecules comprising an icosahedral dodecaborate of B12(OR)12, where R is a perfluoroaryl terminated linker.
3. The molecular scaffold of claim 2, wherein the dodecaborate is perfunctionalized with one or more substituted aromatic perfunctionalization groups, and each of the perfluoraryl terminated linkers is attached to the dodecaborate through said perfunctionalization groups.
4. The molecular scaffold of claim 2, wherein one or more of the fluorine atoms of the perfluoroaryl terminated linkers is substituted with a thiol-containing molecule or macromolecule.
5. The molecular scaffold of claim 4, wherein the thiol-containing macromolecule is a peptide such that the molecular scaffold is an organomimetic cluster nanomolecule.
6. The molecular scaffold of claim 2, wherein the molecular scaffold is PEGylated.
7. The molecular scaffold of claim 4, wherein the thiol-containing molecule is a recognition moiety.
8. The molecular scaffold of claim 7, wherein the recognition moieties are glycoconjugates.
9. The molecular scaffold of claim 8, wherein the glycoconjugates are linked with one or more molecules selected from the group consisting of proteins, peptides, lipid and saccharides.
10. The molecular scaffold of claim 7, wherein the molecular scaffold forms an organomimetic cluster nanomolecule that functions as one of an antibody, protein, histone or viral mimic.
11. The molecular scaffold of claim 10, wherein the molecular scaffold further comprises a viral scaffold and at least one fluorescent moiety, and wherein the molecular scaffold operates as a viral assay.
12. The molecular scaffold of claim 11, wherein the viral scaffold is a gp41 viral scaffold.
13. The molecular scaffold of claim 10, wherein the histone mimic comprises a periodic arrangement of cationic lysine residues separated by one or more helix-promoting hydrophobic amino acids.
| 2017143348 | August 2017 | WO |
| 2017143348 | August 2017 | WO |
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Type: Grant
Filed: Feb 21, 2017
Date of Patent: Oct 25, 2022
Patent Publication Number: 20190047871
Assignee: The Regents of the University of California (Oakland, CA)
Inventors: Alexander Spokoyny (Oakland, CA), Heather D. Maynard (Oakland, CA), Elaine A. Qian (Oakland, CA), Marco S. Messina (Oakland, CA), Alex Wixtrom (Oakland, CA), Jonathan Axtell (Oakland, CA), Kent Kirlikovali (Oakland, CA), Alejandra Gonzalez (Oakland, CA)
Primary Examiner: Yong L Chu
Application Number: 16/077,415
